FDA Inspection 607321 — Coloplast Hungary, KFT.
The FDA completed an inspection of Coloplast Hungary, KFT. on Jun 25, 2009 in Nyirbator. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Devices.
Inspection details
- Classification
- Official Action Indicated (OAI)
- End Date
- Jun 25, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Nyirbator (Hungary)