FDA Inspection 574847 — Ansell (Thailand), Ltd.

Ansell (Thailand), Ltd. — FEI 3002806370

The FDA completed an inspection of Ansell (Thailand), Ltd. on February 26, 2009 in Bangkok. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 26, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Bangkok (Thailand)