FDA Inspection 745134 — Grunenthal GmbH
The FDA completed an inspection of Grunenthal GmbH on Sep 6, 2011 in Aachen. 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 6, 2011
- Fiscal Year
- 2011
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Aachen (Germany)