FDA Inspection 1099839 — Nippon Shikizai, Inc.

Nippon Shikizai, Inc. — FEI 3012051074

The FDA completed an inspection of Nippon Shikizai, Inc. on Aug 6, 2019 in Tsukuba. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Aug 6, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Tsukuba (Japan)

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