FDA Inspection 1100326 — Integra Neurosciences

Integra Neurosciences — FEI 3000204775

The FDA completed an inspection of Integra Neurosciences on August 23, 2019 in Anasco, PR. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 5 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 23, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Anasco, PR (United States)

Citations

IDCFRDescription
310221 CFR 820.30(h)Design transfer - Lack of or inadequate procedures
312521 CFR 820.80(d)Lack of or inadequate final acceptance procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures
54621 CFR 820.75(a)Lack of or inadequate process validation