FDA Inspection 1151851 — Croda Europe Limited

Croda Europe Limited — FEI 3004322377

The FDA completed an inspection of Croda Europe Limited on February 13, 2020 in Leek. 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 13, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Leek (United Kingdom)

Additional Details

Mutual Recognition Agreement (MRA)