FDA Inspection 987027 — Dr. Babor GmbH & Co. KG
The FDA completed an inspection of Dr. Babor GmbH & Co. KG on Aug 11, 2016 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
- Aug 11, 2016
- Fiscal Year
- 2016
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Aachen (Germany)