FDA Warning Letter — Ropack, Inc. (Site A & B)

Case 499580 — FEI 3002674295

The FDA took a Warning Letter action against Ropack, Inc. (Site A & B) on Aug 3, 2016 (Anjou, Canada). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action details

Facility
Ropack, Inc. (Site A & B)
Date
Aug 3, 2016
Fiscal Year
2016
Product Type
Devices
Center
CDRH
Location
Anjou (Canada)

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