FDA Inspection 763376 — Novum Medical Products of NY, LLC

Novum Medical Products of NY, LLC — FEI 1318843

The FDA completed an inspection of Novum Medical Products of NY, LLC on January 13, 2012 in Amherst, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 6 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
January 13, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Amherst, NY (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
1472221 CFR 820.40Procedures not adequately established or maintained
313021 CFR 820.100(a)Lack of or inadequate procedures
315921 CFR 820.184DHR content
317221 CFR 820.198(c)Investigation of device failures
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures