FDA Inspection 1148651 — AndersonBrecon (UK) Limited

AndersonBrecon (UK) Limited — FEI 3001670824

The FDA completed an inspection of AndersonBrecon (UK) Limited on June 27, 2019 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
June 27, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Hereford (United Kingdom)

Additional Details

Mutual Recognition Agreement (MRA)