FDA Inspection 1031035 — AvKARE

AvKARE — FEI 3007255004

The FDA completed an inspection of AvKARE on June 6, 2017 in Pulaski, TN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 6, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Pulaski, TN (United States)