FDA Inspection 733663 — AMBU Limited

AMBU Limited — FEI 3003924186

The FDA completed an inspection of AMBU Limited on June 2, 2011 in Xia Men. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 2, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Xia Men (China)

Citations

IDCFRDescription
312821 CFR 820.90(a)Nonconforming product control
313021 CFR 820.100(a)Lack of or inadequate procedures