What is the FEI / inspection ID for this Form 483?

FEI / inspection ID: 3041017461.

Is a Form 483 the same as a Warning Letter?

No. A Form 483 lists an FDA investigator’s observations at the close of an inspection; it is not a final agency determination. FDA may or may not follow up with a Warning Letter depending on the firm’s response and the severity of the findings.

Where can I read the full Form 483?

The verbatim inspection record is the source of truth — always confirm citation language against the original FDA document before acting.

What is an FDA Form 483?

A Form FDA 483 lists an FDA investigator's written observations at the close of a facility inspection, issued under section 704(b) of the Federal Food, Drug, and Cosmetic Act. It documents conditions the investigator judged may violate FDA regulations. A 483 is not an enforcement action or a final determination that a violation occurred.

FDA Inspects Pure Indulgence Aesthetics: Form 483 with 1 Citations (December 12, 2025)

At a glance: FDA inspected Pure Indulgence Aesthetics in United States and issued a Form 483 listing 1 inspectional observation following an inspection that concluded 2025-12-12. FDA records classify Pure Indulgence Aesthetics as a dispenser of prescription drugs. A Form 483 documents an investigator's findings at the close of an inspection under the Federal Food, Drug, and Cosmetic Act; it is not a final agency compliance determination. The observations on this page are drawn directly from the FDA-issued Form 483 record.

Key facts

Firm	Pure Indulgence Aesthetics
FEI / inspection ID	3041017461
Inspection end date	December 12, 2025
Citation count	1

Citations explained

Observation 1 — DEPARTMENT OF HEALTH AND HUMAN SERVICES FOOD AND DRUG ADMINISTRATION DISTRICT ADDRESS

DEPARTMENT OF HEALTH AND HUMAN SERVICES FOOD AND DRUG ADMINISTRATION DISTRICT ADDRESS AND PHONE NUMBER DATE(S) OF INSPECTION 1201 Main St., Suite 7000 12/02/2025-12/ 12/2025* FEINUMBER Dallas. TX 75202 (2 14) 253-5200 3041017461 NAME AND TITLE OF INDIVIDUAL TO WHOM REPORT ISSUED TO: Bridge tt M. Go ddard, Mana g er FIRMNAME STREET ADDRESS Pure Indulgence Aesthetics 1695 E. Southlake Blvd., Unit 150 CITY, STATE, ZIP CODE, COUNTRY TYPE ESTABLISHMENT INSPECTED Southlake, Texas, 76092 Dispenser of Prescriotion Dm~s This document lists observations made by the FDA representative(s) during the inspection of your facility. They are inspectional observations, and do not represent a final Agency dete

What a Form 483 means

A Form FDA 483 is issued at the close of an FDA facility inspection to list conditions an investigator observed that may violate the Federal Food, Drug, and Cosmetic Act or its implementing regulations. It reflects the investigator's professional judgment at that point in time and is not a final agency determination, an enforcement action, or proof that a violation occurred. Firms are expected to respond in writing, typically within 15 business days, describing the corrective and preventive actions they plan to take. FDA reviews that response, along with any follow-up evidence, before deciding what happens next. Many 483s are resolved through corrective action alone. When FDA judges a firm's response inadequate, or when the underlying conditions are serious enough, the observations documented here can lead to a Warning Letter or further regulatory action. This page presents the observations exactly as recorded on the FDA-issued document; always confirm citation language against the original record before relying on it.

Pure Indulgence Aesthetics’s FDA history

Argus HQ has recorded 1 total FDA action tied to Pure Indulgence Aesthetics: 0 warning letters, 0 recalls, 0 approval records, and 1 Form 483 inspection citation.

Frequently asked questions

What is the FEI / inspection ID for this Form 483?: FEI / inspection ID: 3041017461.
Is a Form 483 the same as a Warning Letter?: No. A Form 483 lists an FDA investigator’s observations at the close of an inspection; it is not a final agency determination. FDA may or may not follow up with a Warning Letter depending on the firm’s response and the severity of the findings.
Where can I read the full Form 483?: The verbatim inspection record is the source of truth — always confirm citation language against the original FDA document before acting.
What is an FDA Form 483?: A Form FDA 483 lists an FDA investigator's written observations at the close of a facility inspection, issued under section 704(b) of the Federal Food, Drug, and Cosmetic Act. It documents conditions the investigator judged may violate FDA regulations. A 483 is not an enforcement action or a final determination that a violation occurred.

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Full FDA history for Pure Indulgence Aesthetics

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.

APA

Argus HQ Research (2025). FDA Inspects Pure Indulgence Aesthetics: Form 483 with 1 Citations (December 12, 2025). Digital Empire LLC. Retrieved from https://argushq.ai/483/fda-483-pure-indulgence-aesthetics-2025-12-12-3041017461

MLA

"FDA Inspects Pure Indulgence Aesthetics: Form 483 with 1 Citations (December 12, 2025)." Argus HQ Research, Digital Empire LLC, 2025, argushq.ai/483/fda-483-pure-indulgence-aesthetics-2025-12-12-3041017461.

Chicago

Argus HQ Research. "FDA Inspects Pure Indulgence Aesthetics: Form 483 with 1 Citations (December 12, 2025)." Digital Empire LLC. Accessed July 13, 2026. https://argushq.ai/483/fda-483-pure-indulgence-aesthetics-2025-12-12-3041017461.

BibTeX

@misc{argushq_argushq_ai_483_fda_483_pure_indulgence_aesthetics_2025_12_12_3041017461_2025,
  title = {FDA Inspects Pure Indulgence Aesthetics: Form 483 with 1 Citations (December 12, 2025)},
  author = {{Argus HQ Research}},
  year = {2025},
  publisher = {Digital Empire LLC},
  url = {https://argushq.ai/483/fda-483-pure-indulgence-aesthetics-2025-12-12-3041017461},
  note = {Accessed: July 13, 2026}
}

Source: FDA.gov — Inspection Classification Database ↗