FDA Inspection 1166312 — CDG BIOTECH

CDG BIOTECH — FEI 3013023580

The FDA completed an inspection of CDG BIOTECH on Mar 21, 2022 in Westlake Village, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 21, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Westlake Village, CA (United States)