FDA Inspection 1214394 — Microcision LLC

Microcision LLC — FEI 1000522098

The FDA completed an inspection of Microcision LLC on August 9, 2023 in Pennsauken, NJ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 4 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 9, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Pennsauken, NJ (United States)

Citations

IDCFRDescription
1471221 CFR 820.184DHR - not or inadequately maintained
313021 CFR 820.100(a)Lack of or inadequate procedures
333121 CFR 820.181DMR - not or inadequately maintained
54621 CFR 820.75(a)Lack of or inadequate process validation