FDA Inspection 890470 — Bioreliance Ltd.

Bioreliance Ltd. — FEI 3005343934

The FDA completed an inspection of Bioreliance Ltd. on July 16, 2014 in Glasgow. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 16, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Glasgow (United Kingdom)