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483
•The Procter & Gamble Manufacturing Company•November 17, 2017

The Procter & Gamble Manufacturing Company – FDA 483, Nov 17, 2017

Record Details

The FDA inspected The Procter & Gamble Manufacturing Company in Greensboro, NC, an OTC drug manufacturer. The inspection revealed significant deficiencies across multiple areas, including a lack of process validation for packaging and labeling, inadequate supplier qualification, and poor complaint handling procedures. Additionally, the firm failed to properly maintain and sanitize equipment and utensils, leading to potential contamination risks.

Company
The Procter & Gamble Manufacturing Company
Inspection date
November 17, 2017
Product type
drugs
Office
Atlanta District Office
People
  • Tajah L. Blackburn (investigator)
  • Susan O. Oladeji
View Company Profile

ID · 7135b04c-f517-4517-88cd-2dc0c2af670b

Other documents for The Procter & Gamble Manufacturing Company
  • 483 - 2023-03-10March 10, 2023
  • EIR - 2023-03-10March 10, 2023

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