FDA Inspection 1072822 — Butterworth Laboratories Ltd

Butterworth Laboratories Ltd — FEI 3002806533

The FDA completed an inspection of Butterworth Laboratories Ltd on August 9, 2017 in Teddington. 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
August 9, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Teddington (United Kingdom)

Additional Details

Mutual Recognition Agreement (MRA)