FDA Inspection 770457 — Dymax Corp
The FDA completed an inspection of Dymax Corp on Mar 2, 2012 in Zelienople, PA. 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 2, 2012
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Zelienople, PA (United States)