FDA Inspection 810043 — Rolence Ent. Inc.
The FDA completed an inspection of Rolence Ent. Inc. on November 15, 2012 in Chungli. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- November 15, 2012
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Chungli (Taiwan)