FDA Inspection 1027604 — Ropack, Inc. (Site A & B)
The FDA completed an inspection of Ropack, Inc. (Site A & B) on July 20, 2017 in Anjou. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- July 20, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Anjou (Canada)