FDA Inspection 1190819 — Avantor Performance Materials Poland S.A.

Avantor Performance Materials Poland S.A. — FEI 3011558129

The FDA completed an inspection of Avantor Performance Materials Poland S.A. on Sep 28, 2022 in Gliwice. 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
Sep 28, 2022
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Gliwice (Poland)

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