FDA Inspection 1122378 — Lofthouse of Fleetwood Ltd.

Lofthouse of Fleetwood Ltd. — FEI 3000291907

The FDA completed an inspection of Lofthouse of Fleetwood Ltd. on August 24, 2018 in Fleetwood. 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 24, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Fleetwood (United Kingdom)

Additional Details

Mutual Recognition Agreement (MRA)