FDA Inspection 1034026 — Dr. Japan Co., Ltd.
The FDA completed an inspection of Dr. Japan Co., Ltd. on November 9, 2017 in Gyoda. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.
Inspection Details
- Classification
- Official Action Indicated (OAI) (OAI)
- End Date
- November 9, 2017
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Gyoda (Japan)