FDA Inspection 1162212 — Harmac Medical Products, Inc.

Harmac Medical Products, Inc. — FEI 1317547

The FDA completed an inspection of Harmac Medical Products, Inc. on February 11, 2022 in Buffalo, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 11, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Buffalo, NY (United States)

Citations

IDCFRDescription
311721 CFR 820.70(i)Software validation for automated processes
313021 CFR 820.100(a)Lack of or inadequate procedures