FDA Inspection 781873 — Shiseido Co.

Shiseido Co. — FEI 3009552960

The FDA completed an inspection of Shiseido Co. on Apr 16, 2012 in Kamakura. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Apr 16, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Kamakura (Japan)

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