FDA Inspection 1099839 — Nippon Shikizai, Inc.

Nippon Shikizai, Inc. — FEI 3012051074

The FDA completed an inspection of Nippon Shikizai, Inc. on August 6, 2019 in Tsukuba. 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
August 6, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Tsukuba (Japan)