FDA Inspection 1029785 — Avantor Performance Materials Poland S.A.
The FDA completed an inspection of Avantor Performance Materials Poland S.A. on Sep 26, 2017 in Gliwice. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Sep 26, 2017
- Fiscal Year
- 2017
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Gliwice (Poland)