FDA Inspection 1113312 — Bentec Medical, Inc.

Bentec Medical, Inc. — FEI 2939142

The FDA completed an inspection of Bentec Medical, Inc. on September 9, 2019 in Woodland, 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
September 9, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Woodland, CA (United States)