FDA Inspection 933520 — Dr. Japan Co., Ltd.
The FDA completed an inspection of Dr. Japan Co., Ltd. on June 28, 2015 in Gyoda. 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
- June 28, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Gyoda (Japan)