FDA Inspection 971718 — Identipak Inc

Identipak Inc — FEI 3002422294

The FDA completed an inspection of Identipak Inc on June 8, 2016 in Mcallen, TX. 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 8, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Mcallen, TX (United States)