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FDA Inspection
•Allure Labs, Inc.•November 22, 2010

Allure Labs, Inc. – FDA Inspection, Nov 22, 2010

Record Details

This FDA Inspection record concerns Allure Labs, Inc., with an inspection on November 22, 2010, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Allure Labs, Inc.
Inspection Date
November 22, 2010
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 63a640f1-15bc-48fa-876a-0af66f89bdca

Inspection Facts

Official Action Indicated (OAI)

Significant objectionable conditions were found and regulatory or administrative action is recommended.

Inspection number
695241
FDA center
Human Drugs
Project area
Drug Quality Assurance

FDA Citations

21
  1. 21 CFR 211.103Actual vs. theoretical yields not determined
  2. 21 CFR 211.100(b)Procedure Deviations Recorded and Justified
  3. 21 CFR 211.142(a)Quarantine - actual practice
  4. 21 CFR 211.165(f)Failing drug products not rejected
  5. 21 CFR 211.165(b)Microbiological testing
  6. 21 CFR 211.84(d)(2)Testing Each Component for Conformity with Specs
  7. 21 CFR 211.80(d)Identification of Each Lot in Each Shipment
  8. 21 CFR 211.25(a)Training--operations, GMPs, written procedures
  9. 21 CFR 211.67(a)Cleaning / Sanitizing / Maintenance
  10. 21 CFR 211.84(e)Rejecting When Specifications Not Met

Showing 10 of 21 citations.

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Allure Labs, Inc.

9
DateClassificationOfficeProject area
March 27, 2026Not classifiedSan Francisco District OfficeDrug Quality Assurance
April 18, 2025VAICenter for Food Safety and Applied NutritionColors and Cosmetics Technology
December 3, 2021VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 23, 2020OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
October 25, 2017VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 9 other inspections on the company page
Other documents for Allure Labs, Inc.
  • FDA Inspection 1310038 - 2026-03-27
  • FDA Inspection 1267803 - 2025-04-18
  • FDA Inspection 1158759 - 2021-12-03
  • FDA Inspection 1133603 - 2020-11-23
  • FDA Inspection 1030713 - 2017-10-25

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