FDA Inspection 618247 — Ansynth Service BV
The FDA completed an inspection of Ansynth Service BV on September 18, 2009 in Breda. 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
- September 18, 2009
- Fiscal Year
- 2009
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Breda (Netherlands)