FDA Inspection 747338 — Kinkando Co., Ltd.

Kinkando Co., Ltd. — FEI 3004016987

The FDA completed an inspection of Kinkando Co., Ltd. on Sep 2, 2011 in Honjo. 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
Sep 2, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Honjo (Japan)

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