FDA Inspection 898000 — Almirall Hermal GmbH
The FDA completed an inspection of Almirall Hermal GmbH on Sep 26, 2014 in Reinbek. 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, 2014
- Fiscal Year
- 2014
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Reinbek (Germany)