FDA Inspection 1079100 — ALC Enterprises Inc.

ALC Enterprises Inc. — FEI 3011721071

The FDA completed an inspection of ALC Enterprises Inc. on February 13, 2019 in Brooklyn, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 13, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Brooklyn, NY (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
63021 CFR 803.17Lack of Written MDR Procedures