FDA Inspection 756447 — Accumedix, Inc.

Accumedix, Inc. — FEI 3003473212

The FDA completed an inspection of Accumedix, Inc. on December 5, 2011 in Libertyville, IL. 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
December 5, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Libertyville, IL (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures