FDA Inspection 1003818 — Unipack LLC

Unipack LLC — FEI 3008275696

The FDA completed an inspection of Unipack LLC on March 2, 2017 in South Plainfield, NJ. 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
March 2, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
South Plainfield, NJ (United States)