FDA Inspection 1079443 — Nipro Medical Industries, Ltd.
The FDA completed an inspection of Nipro Medical Industries, Ltd. on November 15, 2018 in Tatebayashi. 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, 2018
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Tatebayashi (Japan)