FDA Inspection 1018218 — Collagen Matrix Inc

Collagen Matrix Inc — FEI 3008817245

The FDA completed an inspection of Collagen Matrix Inc on July 18, 2017 in Oakland, NJ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 18, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Oakland, NJ (United States)

Citations

IDCFRDescription
319021 CFR 820.30(g)Design validation acceptance criteria
342621 CFR 820.50(a)(1)Documented evaluation
369621 CFR 820.100(b)Documentation