FDA Inspection 1338568 — SHISEIDO AMERICAS CORPORATION

SHISEIDO AMERICAS CORPORATION — FEI 3012334331

The FDA completed an inspection of SHISEIDO AMERICAS CORPORATION on Aug 21, 2026 in Groveport, OH. 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
Aug 21, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Groveport, OH (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.