FDA Inspection 1020601 — NANIWA CO., LTD.
The FDA completed an inspection of NANIWA CO., LTD. on June 29, 2017 in Miyoshi. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Food/Cosmetics.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- June 29, 2017
- Fiscal Year
- 2017
- Product Type
- Food/Cosmetics
- Project Area
- Foodborne Biological Hazards
- Location
- Miyoshi (Japan)