FDA Inspection 886286 — Ansynth Service BV

Ansynth Service BV — FEI 3004827681

The FDA completed an inspection of Ansynth Service BV on June 20, 2014 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
June 20, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Breda (Netherlands)