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FDA Inspection
•Olay LLC•July 22, 2013

Olay LLC – FDA Inspection, Jul 22, 2013

Record Details

This FDA Inspection record concerns Olay LLC, with an inspection on July 22, 2013, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Olay LLC
Inspection Date
July 22, 2013
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 593063c8-8a86-4fbe-8c67-37671e63b902

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
850745
FDA center
Human Drugs
Project area
Drug Quality Assurance

FDA Citations

3
  1. 21 CFR 211.67(c)Cleaning/maintenance records not kept
  2. 21 CFR 211.170(b)Annual visual exams of drug products
  3. 21 CFR 211.22(d)Procedures not in writing, fully followed

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Olay LLC

5
DateClassificationOfficeProject area
October 21, 2015NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 18, 2012VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 22, 2010VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 12, 2008OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
October 1, 2008OAICenter for Food Safety and Applied NutritionColors and Cosmetics Technology
Other documents for Olay LLC
  • FDA Inspection 947105 - 2015-10-21
  • FDA Inspection 777753 - 2012-04-18
  • FDA Inspection 698850 - 2010-11-22
  • FDA Inspection 550070 - 2008-11-12
  • FDA Inspection 542404 - 2008-10-01

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