Key facts
| Company | Golden Dakota Farms LLC |
|---|---|
| FDA office | Center for Veterinary Medicine |
| Letter date | May 20, 2026 |
| Subject / product | New Animal Drug/Adulterated |
| CFR citations | FDA Warning Letter |
| Response due | 15 working days from receipt (standard FDA warning-letter requirement) |
| Reference / source ID | golden-dakota-farms-llc-725317-05202026 |
Violations explained
FDA Warning Letter — Violations FDA cited at Golden Dakota Farms LLC
WARNING LETTER Golden Dakota Farms LLC MARCS-CMS 725317 — May 20, 2026 More Warning Letters Warning Letters About Warning and Close-Out Letters Delivery Method: Via Email Product: Animal & Veterinary Recipient: Recipient Name Nicholas Coetzee, Owner Recipient Title Eric Goedhart, Owner Golden Dakota Farms LLC 48188 221st Street Elkton , SD 57026-5059 United States (b)(6), (b)(7)(C) Issuing Office: Center for Veterinary Medicine United States WARNING LETTER CMS # 725317 May 20, 2026 Dear Messrs. Coetzee and Goedhart, The United States Food and Drug Administration (FDA) conducted an inspection of your dairy operation located at 48188 221st Street, Elkton, South Dakota, between January 26 and January 29, 2026. This letter notifies you of violations of the Federal Food, Drug, and Cosmetic Act (FD&C Act) that were revealed during the inspection. At the close of the inspection, you were issued a Form FDA 483, Inspectional Observations (FDA 483). We acknowledge your written response received February 11, 2026, and address your proposed corrections below. You can find the FD&C Act and its associated regulations on the internet through links on the FDA’s web page at www.fda.gov. Adulteration of an Animal Offered for Human Consumption Our inspection found you offered for sale a dairy cow for slaughter as food that was adulterated. Specifically, on (b)(4) , you sold a dairy cow identified with ear tag (b)(4) . This cow was slaughtered to be used as food at (b)(4) in (b)(4) on (b)(4) . United States Department of Agriculture/Food Safety Inspection Services (USDA/FSIS) analysis of edible tissue revealed the presence of ampicillin at 1.68 parts per million (ppm) in muscle tissue and 0.0898 ppm in kidney tissue. Additionally, on (b)(4) , you sold a dairy cow identified with ear tag (b)(4) . This cow was slaughtered to be used as food at (b)(4) in (b)(4) on (b)(4) . USDA/FSIS analysis of kidney tissue revealed the presence of ampicillin at 0.0242 ppm. FDA has established a tolerance of 0.01 ppm of ampicillin in edible tissue for cattle. 1 The presence of this drug in edible tissue from animals at these levels cause the food to be adulterated. A food is deemed adulterated if it bears or contains a new animal drug that is unsafe. 2 A drug is unsafe if it results in any residues that exceed established safe levels. 3 Additionally, our investigation found that you hold animals under insanitary conditions that are inadequate such that medicated animals bearing potentially harmful drug residues are likely to enter the food supply. Specifically, you did not maintain complete and accurate treatment records for cattle that you medicate: You had no records documenting you treated a dairy cow with ear tag (b)(4) using antibiotics. You indicated that you may have treated the cow in error with (b)(4) . The cow with ear tag (b)(4) was sold for slaughter for human food on (b)(4) , and found to contain a violative ampicillin residue in kidney tissue at the time of slaughter on (b)(4). You do not maintain complete treatment records. You administered (b)(4) to a dairy cow with ear tag (b)(4) from (b)(4) , without documenting the dosage in your treatment records. The cow was sold on (b)(4) , and was later found to contain a violative ampicillin residue in muscle tissue and kidney tissue at the time of slaughter on (b)(4) . Food held under insanitary conditions whereby it may have been rendered injurious to health is adulterated. 4 The introduction or delivery for introduction into interstate commerce of any food that is adulterated is a prohibited act. 5 Adulteration of a New Animal Drug Our inspection found that you did not use (b)(4) , as directed by the drug manufacturer’s approved labeling and your veterinarian’s prescription labels. Use of a drug in a manner that is not consistent with its labeling is an extralabel use. 6 Our inspection found you administered (b)(4) concentration to treat a dairy cow with ear tag (b)(4) from (b)(4) , for a difficult birth
What happens next
Golden Dakota Farms LLC is expected to respond to FDA in writing, typically within 15 working days of the letter date, describing the specific corrective and preventive actions taken or planned for each violation cited. FDA reviews that response and any follow-up evidence, and can conduct a re-inspection to confirm the corrections were actually made. If FDA judges the response inadequate, or the underlying conditions serious enough, further action can follow, including product seizure, injunction, import alert, or civil penalties; many Warning Letters are resolved through corrective action alone. This page reflects the Warning Letter as issued and will not reflect any subsequent correction unless FDA publishes a follow-up record. FDA issues Warning Letters after an inspection or other review when it believes a firm has significantly violated FDA regulations; the letter itself is a notice, not a final adjudication.
Golden Dakota Farms LLC’s FDA history
Argus HQ has recorded 1 total FDA action tied to Golden Dakota Farms LLC: 1 warning letter, 0 recalls, 0 approval records, and 0 Form 483 inspection citations.
Full letter text
Read the rest of the full text
Frequently asked questions
- What CFR citations does this warning letter reference?
- The letter cites: FDA Warning Letter.
- Is the FDA warning letter to Golden Dakota Farms LLC publicly available?
- Yes. The full verbatim letter is published at fda.gov: https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/golden-dakota-farms-llc-725317-05202026.
- What is the standard FDA response window for a warning letter?
- FDA warning letters typically require a written response within 15 working days of receipt, outlining the corrective and preventive actions the company will take.
- What is an FDA Warning Letter?
- An FDA Warning Letter notifies a company that FDA believes it has significantly violated FDA regulations and that prompt corrective action is required. It is issued after an inspection, sample analysis, or other FDA review, and is a notice -- not a final legal determination and not itself a penalty.
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Compiled by Argus HQ Research from FDA primary sources · Reviewed by Andy Gaber, Founder
Cite this record
Reusing this data in reporting or research? Here’s a ready-made citation.
Argus HQ Research (2026). Warning Letter Record: Golden Dakota Farms LLC (May 20, 2026) — New Animal Drug/Adulterated. Digital Empire LLC. Retrieved from https://argushq.ai/warning-letter/golden-dakota-farms-725317-2026-05-20
"Warning Letter Record: Golden Dakota Farms LLC (May 20, 2026) — New Animal Drug/Adulterated." Argus HQ Research, Digital Empire LLC, 2026, argushq.ai/warning-letter/golden-dakota-farms-725317-2026-05-20.
Argus HQ Research. "Warning Letter Record: Golden Dakota Farms LLC (May 20, 2026) — New Animal Drug/Adulterated." Digital Empire LLC. Accessed July 13, 2026. https://argushq.ai/warning-letter/golden-dakota-farms-725317-2026-05-20.
@misc{argushq_argushq_ai_warning_letter_golden_dakota_farms_725317_2026_05_20_2026,
title = {Warning Letter Record: Golden Dakota Farms LLC (May 20, 2026) — New Animal Drug/Adulterated},
author = {{Argus HQ Research}},
year = {2026},
publisher = {Digital Empire LLC},
url = {https://argushq.ai/warning-letter/golden-dakota-farms-725317-2026-05-20},
note = {Accessed: July 13, 2026}
}Source: FDA.gov — Warning Letters ↗

