FDA Inspection 718574 — Prodimed
The FDA completed an inspection of Prodimed on Mar 17, 2011 in Neuilly En Thelle. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Mar 17, 2011
- Fiscal Year
- 2011
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Neuilly En Thelle (France)