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FDA Inspection
•The Procter & Gamble Manufacturing Company•July 18, 2013

The Procter & Gamble Manufacturing Company – FDA Inspection, Jul 18, 2013

Record Details

This FDA Inspection record concerns The Procter & Gamble Manufacturing Company, with an inspection on July 18, 2013, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
The Procter & Gamble Manufacturing Company
Inspection Date
July 18, 2013
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · dd1a35c7-c6d8-4f17-8eca-9d939f2b6745

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
842993
FDA center
Human Drugs
Project area
Drug Quality Assurance

FDA Citations

1
  1. 21 CFR 211.194(d)Laboratory equipment calibration records

Full citation text and observation details available on the Dashboard.

Other FDA inspections of The Procter & Gamble Manufacturing Company

6
DateClassificationOfficeProject area
June 9, 2026Not classifiedAtlanta District OfficeDrug Quality Assurance
March 10, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 17, 2017VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 6, 2016NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 5, 2010VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 6 other inspections on the company page
Other documents for The Procter & Gamble Manufacturing Company
  • FDA Inspection 1311376 - 2026-06-09
  • FDA Inspection 1199458 - 2023-03-10
  • FDA Inspection 1031577 - 2017-11-17
  • FDA Inspection 984572 - 2016-05-06
  • FDA Inspection 654299 - 2010-02-05

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