FDA Inspection 1214917 — AccuMED Corp.

AccuMED Corp. — FEI 3007309299

The FDA completed an inspection of AccuMED Corp. on July 20, 2023 in Nigua. 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
July 20, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Nigua (Dominican Republic (the))

Citations

IDCFRDescription
54621 CFR 820.75(a)Lack of or inadequate process validation