FDA Inspection 868322 — Coloplast Hungary, KFT.
The FDA completed an inspection of Coloplast Hungary, KFT. on Mar 4, 2014 in Nyirbator. 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 4, 2014
- Fiscal Year
- 2014
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Nyirbator (Hungary)