FDA Inspection 545831 — Ropack, Inc. (Site A & B)

Ropack, Inc. (Site A & B) — FEI 3002674295

The FDA completed an inspection of Ropack, Inc. (Site A & B) on October 21, 2008 in Anjou. 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
October 21, 2008
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Anjou (Canada)