FDA Inspection 890477 — Bioreliance Ltd.

Bioreliance Ltd. — FEI 3005619549

The FDA completed an inspection of Bioreliance Ltd. on Jul 18, 2014 in Stirling, Scotland. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Jul 18, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Stirling, Scotland (United Kingdom)

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