FDA Inspection 694678 — Tomita Pharmaceutical Co., Ltd.

Tomita Pharmaceutical Co., Ltd. — FEI 3002808375

The FDA completed an inspection of Tomita Pharmaceutical Co., Ltd. on September 10, 2010 in Naruto. 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
September 10, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Naruto (Japan)