FDA Inspection 928373 — Seirin Corporation
The FDA completed an inspection of Seirin Corporation on May 14, 2015 in Shizuoka-Shi. 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
- May 14, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Shizuoka-Shi (Japan)