FDA Inspection 781834 — CooperVision Limited

CooperVision Limited — FEI 3002807783

The FDA completed an inspection of CooperVision Limited on May 17, 2012 in Eastleigh. 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). 1 citation was issued during this inspection. Product area: Devices.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
May 17, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Eastleigh (United Kingdom)

Citations

IDCFRDescription
235021 CFR 820.25(b)Training - Lack of or inadequate procedures

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