FDA Inspection 1056805 — Harmac Medical Products, Inc.

Harmac Medical Products, Inc. — FEI 1317547

The FDA completed an inspection of Harmac Medical Products, Inc. on June 21, 2018 in Buffalo, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 21, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Buffalo, NY (United States)

Citations

IDCFRDescription
54121 CFR 820.70(c)Environmental control Lack of or inadequate procedures