FDA Inspection 907474 — Shiono Finesse, Ltd.

Shiono Finesse, Ltd. — FEI 3005940219

The FDA completed an inspection of Shiono Finesse, Ltd. on Nov 7, 2014 in Sakai. 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
Nov 7, 2014
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sakai (Japan)

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