FDA Inspection 1314106 — AMBU Limited

AMBU Limited — FEI 3003924186

The FDA completed an inspection of AMBU Limited on Apr 16, 2026 in Xia Men. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Apr 16, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Xia Men (China)

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