FDA Inspection 1199458 — The Procter & Gamble Manufacturing Company

The Procter & Gamble Manufacturing Company — FEI 1017175

The FDA completed an inspection of The Procter & Gamble Manufacturing Company on Mar 10, 2023 in Greensboro, NC. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 2 citations were issued during this inspection. Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 10, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Greensboro, NC (United States)

Citations

IDCFRDescription
135821 CFR 211.100(b)SOPs not followed / documented
180221 CFR 211.84(b)Representative Samples

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.