FDA Inspection 885871 — Delpharm Meppel B.V.
The FDA completed an inspection of Delpharm Meppel B.V. on Jun 27, 2014 in Meppel. 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
- Jun 27, 2014
- Fiscal Year
- 2014
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Meppel (Netherlands)