FDA Inspection 852195 — Millipore (U.K.) Ltd.
The FDA completed an inspection of Millipore (U.K.) Ltd. on Oct 4, 2013 in Livingston. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Biologics.
Inspection details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Oct 4, 2013
- Fiscal Year
- 2014
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Livingston (United Kingdom)