FDA Inspection 920667 — EPSILON IMAGING, INC

EPSILON IMAGING, INC — FEI 3008840981

The FDA completed an inspection of EPSILON IMAGING, INC on Apr 3, 2015 in Ann Arbor, MI. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Apr 3, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Ann Arbor, MI (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