FDA Inspection 716711 — AndersonBrecon (UK) Limited

AndersonBrecon (UK) Limited — FEI 3001670824

The FDA completed an inspection of AndersonBrecon (UK) Limited on February 24, 2011 in Hereford. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 24, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Hereford (United Kingdom)