FDA Inspection 635485 — PAJUNK GMBH MEDIZINTECHNOLOGIE
The FDA completed an inspection of PAJUNK GMBH MEDIZINTECHNOLOGIE on Dec 17, 2009 in Geisingen. 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
- Dec 17, 2009
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Geisingen (Germany)