FDA Inspection 989787 — Poly-Med Inc

Poly-Med Inc — FEI 3006121828

The FDA completed an inspection of Poly-Med Inc on Sep 23, 2016 in Anderson, SC. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 23, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Anderson, SC (United States)

Citations

IDCFRDescription
343321 CFR 820.75(c)Process changes - review, evaluation and revalidation
369621 CFR 820.100(b)Documentation