FDA Inspection 1015629 — bioMerieux, Inc.

bioMerieux, Inc. — FEI 3002769706

The FDA completed an inspection of bioMerieux, Inc. on April 10, 2017 in Durham, NC. 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
April 10, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Durham, NC (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures
342721 CFR 820.50(a)(2)Supplier oversight