FDA Inspection 1084230 — BRIGHTWATER MEDICAL, INC.

BRIGHTWATER MEDICAL, INC. — FEI 3013376034

The FDA completed an inspection of BRIGHTWATER MEDICAL, INC. on Mar 13, 2019 in Temecula, 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 13, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Temecula, CA (United States)