FDA Inspection 1248463 — Dymax Corp

Dymax Corp — FEI 3013041594

The FDA completed an inspection of Dymax Corp on August 23, 2024 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
August 23, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Zelienople, PA (United States)