FDA Inspection 1115204 — 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 November 29, 2019 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
November 29, 2019
Fiscal Year
2020
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Royston (United Kingdom)

Additional Details

Bioanalytical BA/BE