FDA Inspection 939507 — Advanced OrthoPro, Inc.

Advanced OrthoPro, Inc. — FEI 3007912159

The FDA completed an inspection of Advanced OrthoPro, Inc. on Jul 30, 2015 in Indianapolis, IN. 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
Jul 30, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Indianapolis, IN (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures
322421 CFR 820.70(g)(2)Periodic equipment inspection lack of or inadequate procedu

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