FDA Inspection 1032347 — CGR Products MN, LLC.
The FDA completed an inspection of CGR Products MN, LLC. on November 15, 2017 in Inver Grove Heights, MN. 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
- November 15, 2017
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Inver Grove Heights, MN (United States)