FDA Inspection 1147432 — Dymax Corp

Dymax Corp — FEI 3013041594

The FDA completed an inspection of Dymax Corp on July 30, 2021 in Zelienople, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 30, 2021
Fiscal Year
2021
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Zelienople, PA (United States)

Citations

IDCFRDescription
312821 CFR 820.90(a)Nonconforming product control