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FDA Inspection 976630 — BioReliance Limited

BioReliance Limited — FEI 3005619544

The FDA completed an inspection of BioReliance Limited on March 17, 2016 in Penicuik. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 17, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Penicuik (United Kingdom)

Facility

Other inspections at this facility

  • 1225221 (NAI Tue Nov 07 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1091242 (VAI Thu Mar 21 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 989581 (NAI Wed Sep 07 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 890483 (VAI Wed Jul 23 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources