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FDA Inspection 1043191 — Millipore (U.K.) Ltd.

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

The FDA completed an inspection of Millipore (U.K.) Ltd. on February 26, 2018 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
February 26, 2018
Fiscal Year
2018
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))
  • 950740 (VAI Fri Oct 02 2015 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