FDA Inspection 1208592 — Melbourn Scientific Limited (d.b.a. Intertek Melbourn)

Melbourn Scientific Limited (d.b.a. Intertek Melbourn) — FEI 3002807539

The FDA completed an inspection of Melbourn Scientific Limited (d.b.a. Intertek Melbourn) on June 16, 2022 in Royston. 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
June 16, 2022
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Royston (United Kingdom)

Additional Details

Mutual Recognition Agreement (MRA)