FDA Inspection 1057836 — Per Rathenborg
The FDA completed an inspection of Per Rathenborg on May 25, 2018 in Herlev. 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
- May 25, 2018
- Fiscal Year
- 2018
- Product Type
- Drugs
- Project Area
- Bioresearch Monitoring
- Location
- Herlev (Denmark)
Additional Details
Clinical Investigator (CI)