FDA Inspection 1178689 — ITG-Medev, Inc.

ITG-Medev, Inc. — FEI 1000307251

The FDA completed an inspection of ITG-Medev, Inc. on Aug 16, 2022 in San Francisco, 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
Aug 16, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
San Francisco, CA (United States)

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