FDA Inspection 742239 — MIM Software Inc

MIM Software Inc — FEI 3004363352

The FDA completed an inspection of MIM Software Inc on Sep 2, 2011 in Cleveland, OH. 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). 1 citation was issued during this inspection. Product area: Devices.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 2, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Cleveland, OH (United States)

Citations

IDCFRDescription
369621 CFR 820.100(b)Documentation

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