FDA Inspection 1012877 — MedRx, Inc.

MedRx, Inc. — FEI 1000307595

The FDA completed an inspection of MedRx, Inc. on April 25, 2017 in Largo, FL. 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
April 25, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Largo, FL (United States)

Citations

IDCFRDescription
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures