FDA Inspection 770457 — Dymax Corp

Dymax Corp — FEI 3013041594

The FDA completed an inspection of Dymax Corp on March 2, 2012 in Zelienople, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 2, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Zelienople, PA (United States)