FDA Inspection 1107214 — Amphenol DC Electronics Inc.

Amphenol DC Electronics Inc. — FEI 3001763079

The FDA completed an inspection of Amphenol DC Electronics Inc. on Sep 4, 2019 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
Sep 4, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
San Jose, CA (United States)

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