FDA Inspection 890299 — Geon Corporation
The FDA completed an inspection of Geon Corporation on Jul 17, 2014 in Zhang Hua Xian. 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
- Jul 17, 2014
- Fiscal Year
- 2014
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Zhang Hua Xian (Taiwan)