FDA Inspection 1192873 — Amphenol DC Electronics Inc.

Amphenol DC Electronics Inc. — FEI 3001763079

The FDA completed an inspection of Amphenol DC Electronics Inc. on Nov 16, 2022 in San Jose, 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
Nov 16, 2022
Fiscal Year
2023
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
San Jose, CA (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.