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FDA Inspection 950740 — Millipore (U.K.) Ltd.

Millipore (U.K.) Ltd. — FEI 3002638287

The FDA completed an inspection of Millipore (U.K.) Ltd. on October 2, 2015 in Livingston. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
October 2, 2015
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Livingston (United Kingdom)

Facility

Other inspections at this facility

  • 1119027 (VAI Thu Feb 27 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1043191 (VAI Mon Feb 26 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 852195 (VAI Fri Oct 04 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 745585 (NAI Thu Sep 22 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 733480 (VAI Thu Jun 30 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources