FDA Inspection 1155764 — Croda Europe Ltd.

Croda Europe Ltd. — FEI 3004214492

The FDA completed an inspection of Croda Europe Ltd. on Sep 25, 2019 in Widnes. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 25, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Widnes (United Kingdom)

Additional Details

Mutual Recognition Agreement (MRA)

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