FDA Inspection 700365 — Yoneyama Yakuhin Kogyo Co., Ltd.
The FDA completed an inspection of Yoneyama Yakuhin Kogyo Co., Ltd. on November 11, 2010 in Osaka. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- November 11, 2010
- Fiscal Year
- 2011
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Osaka (Japan)