FDA Inspection 810043 — Rolence Ent. Inc.
The FDA completed an inspection of Rolence Ent. Inc. on Nov 15, 2012 in Chungli. 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
- Nov 15, 2012
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Chungli (Taiwan)