FDA Inspection 683803 — Dechra Ltd

Dechra Ltd — FEI 3004499992

The FDA completed an inspection of Dechra Ltd on September 24, 2010 in Skipton. 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
September 24, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Skipton (United Kingdom)