FDA Inspection 1197245 — CDR Manufacturing Inc.

CDR Manufacturing Inc. — FEI 3003857828

The FDA completed an inspection of CDR Manufacturing Inc. on February 2, 2023 in Oakdale, 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
February 2, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Oakdale, MN (United States)