FDA Inspection 1238625 — Amphenol Medical Technologies (Dongguan) Co., Ltd.

Amphenol Medical Technologies (Dongguan) Co., Ltd. — FEI 3013596024

The FDA completed an inspection of Amphenol Medical Technologies (Dongguan) Co., Ltd. on Apr 17, 2024 in Dongguan. 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
Apr 17, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Dongguan (China)

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