FDA Inspection 757196 — Accogent Pausch
The FDA completed an inspection of Accogent Pausch on Dec 14, 2011 in Tinton Falls, NJ. 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 14, 2011
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Tinton Falls, NJ (United States)