FDA Inspection 1172473 — TriReme Medical, LLC.

TriReme Medical, LLC. — FEI 3008089360

The FDA completed an inspection of TriReme Medical, LLC. on June 17, 2022 in Pleasanton, 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
June 17, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Pleasanton, CA (United States)