FDA Inspection 1209998 — Procter & Gamble Manufacturing GmbH

Procter & Gamble Manufacturing GmbH — FEI 3001903296

The FDA completed an inspection of Procter & Gamble Manufacturing GmbH on Mar 15, 2023 in Gros-Gerau. 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). Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 15, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Gros-Gerau (Germany)

Additional details

Mutual Recognition Agreement (MRA)

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