FDA Inspection 844391 — Ropack, Inc. (Site A & B)

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

The FDA completed an inspection of Ropack, Inc. (Site A & B) on Jul 29, 2013 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
Jul 29, 2013
Fiscal Year
2013
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.