FDA Inspection 1018314 — PMC Biogenix, Inc.

PMC Biogenix, Inc. — FEI 1030293

The FDA completed an inspection of PMC Biogenix, Inc. on April 27, 2017 in Memphis, TN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 27, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Memphis, TN (United States)