FDA Inspection 762148 — Ropack, Inc. (Site A & B)

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

The FDA completed an inspection of Ropack, Inc. (Site A & B) on Dec 8, 2011 in Anjou. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Dec 8, 2011
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Anjou (Canada)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.