FDA Inspection 665657 — Coopervision Manufacturing, Ltd.
The FDA completed an inspection of Coopervision Manufacturing, Ltd. on Apr 15, 2010 in Southampton. 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: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Apr 15, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Project Evaluation: Devices
- Location
- Southampton (United Kingdom)
Additional Details
Postmarket Audit Inspections