FDA Inspection 956681 — Deretil, S.A.
The FDA completed an inspection of Deretil, S.A. on January 8, 2016 in Cuevas Del Almanzora. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- January 8, 2016
- Fiscal Year
- 2016
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Cuevas Del Almanzora (Spain)