FDA Inspection 1102101 — USGI Medical, Inc.

USGI Medical, Inc. — FEI 3004447686

The FDA completed an inspection of USGI Medical, Inc. on August 20, 2019 in San Clemente, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 20, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
San Clemente, CA (United States)