Key facts
| Company | Sahara Enterprise Inc. |
|---|---|
| FDA office | Office of Inspections and Investigations |
| Letter date | April 29, 2026 |
| Subject / product | Foreign Supplier Verification Program (FSVP) |
| CFR citations | FDA Warning Letter |
| Response due | 15 working days from receipt (standard FDA warning-letter requirement) |
| Reference / source ID | sahara-enterprise-inc-728927-04292026 |
What happens next
Sahara Enterprise Inc. 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.
Violations explained
FDA Warning Letter — Violations FDA cited at Sahara Enterprise Inc.
WARNING LETTER Sahara Enterprise Inc. MARCS-CMS 728927 — April 29, 2026 More Warning Letters Warning Letters About Warning and Close-Out Letters Delivery Method: Via Email Product: Food & Beverages Recipient: Recipient Name Khalid A. Zaidan Recipient Title Owner Sahara Enterprise Inc. 10981 Decatur Rd. Ste 4 Philadelphia , PA 19154-3213 United States FBOUKHORB@GMAIL.COM Issuing Office: Office of Inspections and Investigations United States April 29, 2026 WARNING LETTER RE: CMS# 728927 Dear Khalid A. Zaidan: On February 27,2026 through March 16,2026, the Food and Drug Administration (FDA) conducted a Foreign Supplier Verification Program (FSVP) inspection of Sahara Enterprise Inc. located at 10981 Decatur Rd., Ste 4, Philadelphia, PA 19154-3213. We also conducted an inspection on November 15, 2018, December 28, 2020, July 28,2022 and September 14,2023. These inspections were conducted to determine compliance with the requirements of section 805 of the Federal Food, Drug, and Cosmetic Act (FD&C Act) (21 U.S.C. 384a) and the implementing FSVP regulation in 21 CFR part 1, subpart L. The FSVP regulation requires that importers perform certain risk-based activities to verify that human and/or animal food they import into the United States has been produced in a manner that meets applicable U.S. food safety standards. You may find information relating to the FSVP regulation and your responsibilities to comply with the regulation through links in FDA’s FSVP web page at https://www.fda.gov/food/food-safety-modernization-act-fsma/fsma-final-rule-foreign-supplier-verification-programs-fsvp-importers-food-humans-and-animals. During the most recent inspection, we found that you are not in compliance with the requirements of 21 CFR part 1, subpart L for the foods you import. Because of these significant violations, you are not in compliance with section 805 of the FD&C Act. At the conclusion of the inspection, our investigator provided you with a Form FDA 483a FSVP Observations. We acknowledge receipt of your response, dated April 07,2026 in which you stated that you will try to learn more on how to prepare FSVP records and also try to get third-party help and prepare FSVP records for the three products. We are unable to evaluate the adequacy of your response because you have not provided any supporting documentation demonstrating your corrective actions. To date, no additional FSVP documents have been received by FDA. Your significant violations of the FSVP regulation are as follows: You did not develop, maintain, and follow an FSVP as required by section 805 of the FD&C Act and 21 CFR 1.502(a). Specifically, you did not develop an FSVP for any of the foods you import, including each of the following foods: 1. DRY DOUGH MIX (phyllo dough) imported from (b)(4) , located in (b)(4) . 2. CANDY (Turkish delight) imported from (b)(4) , located in (b)(4) . 3. BAKLAVA imported from (b)(4) located in (b)(4) . The above violations are not intended to be an all-inclusive list of violations of the FSVP requirements. It is your responsibility to ensure that you are in compliance with section 805 of the FD&C Act and the implementing regulation in 21 CFR part 1, subpart L. This letter notifies you of our concerns and provides you with an opportunity to address them. If you do not adequately address this matter, we may take further action. For instance, we may take action under section 801(a)(3) of the FD&C Act (21 U.S.C. 381(a)(3)) to refuse admission of the food you import for which you appear to be in violation of section 805. We may place the foods you import into the United States on detention without physical examination (DWPE) when you import the foods. You can find DWPE information relating to FSVP in Import Alert # 99-41 at http://www.accessdata.fda.gov/cms_ia/ialist.html. In addition, the importation or offering for importation into the United States of an article of food without the importer having an FSVP that meets the requirements of section
Sahara Enterprise Inc.’s FDA history
Argus HQ has recorded 1 total FDA action tied to Sahara Enterprise Inc.: 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
- Has Sahara Enterprise Inc. had other FDA enforcement actions?
- This is the only FDA action Argus HQ has on file for Sahara Enterprise Inc. so far. Argus ingests new FDA enforcement records daily.
- Which FDA office issued the warning letter to Sahara Enterprise Inc.?
- Office of Inspections and Investigations issued the warning letter to Sahara Enterprise Inc..
- What CFR citations does this warning letter reference?
- The letter cites: FDA Warning Letter.
- Is the FDA warning letter to Sahara Enterprise Inc. publicly available?
- Yes. The full verbatim letter is published at fda.gov: https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/sahara-enterprise-inc-728927-04292026.
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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: Sahara Enterprise Inc. (April 29, 2026) — Foreign Supplier Verification Program (FSVP). Digital Empire LLC. Retrieved from https://argushq.ai/warning-letter/sahara-enterprise-728927-2026-04-29
"Warning Letter Record: Sahara Enterprise Inc. (April 29, 2026) — Foreign Supplier Verification Program (FSVP)." Argus HQ Research, Digital Empire LLC, 2026, argushq.ai/warning-letter/sahara-enterprise-728927-2026-04-29.
Argus HQ Research. "Warning Letter Record: Sahara Enterprise Inc. (April 29, 2026) — Foreign Supplier Verification Program (FSVP)." Digital Empire LLC. Accessed July 13, 2026. https://argushq.ai/warning-letter/sahara-enterprise-728927-2026-04-29.
@misc{argushq_argushq_ai_warning_letter_sahara_enterprise_728927_2026_04_29_2026,
title = {Warning Letter Record: Sahara Enterprise Inc. (April 29, 2026) — Foreign Supplier Verification Program (FSVP)},
author = {{Argus HQ Research}},
year = {2026},
publisher = {Digital Empire LLC},
url = {https://argushq.ai/warning-letter/sahara-enterprise-728927-2026-04-29},
note = {Accessed: July 13, 2026}
}Source: FDA.gov — Warning Letters ↗

