FDA Inspection 1180046 — Biosense Webster, Inc.

Biosense Webster, Inc. — FEI 3013300026

The FDA completed an inspection of Biosense Webster, Inc. on Sep 2, 2022 in Irvine, 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
Sep 2, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Irvine, CA (United States)

Additional Details

Sponsor, Contract Research Organization