FDA Inspection 605846 — Inopak Ltd

Inopak Ltd — FEI 1000122232

The FDA completed an inspection of Inopak Ltd on August 21, 2009 in Ringwood, NJ. 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
August 21, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ringwood, NJ (United States)