FDA Inspection 1274186 — Goodman Co., Ltd. Goodman Research Center / Goodman Medical Innovation Center

Goodman Co., Ltd. Goodman Research Center / Goodman Medical Innovation Center — FEI 3011826338

The FDA completed an inspection of Goodman Co., Ltd. Goodman Research Center / Goodman Medical Innovation Center on May 15, 2025 in Seto. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
May 15, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Project Evaluation: Devices
Location
Seto (Japan)

Additional Details

Postmarket Audit Inspections

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