FDA Inspection 872220 — TriReme Medical, LLC.

TriReme Medical, LLC. — FEI 3008089360

The FDA completed an inspection of TriReme Medical, LLC. on March 6, 2014 in Pleasanton, CA. 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
March 6, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Pleasanton, CA (United States)