FDA Inspection 1269122 — Goodman Co., Ltd

Goodman Co., Ltd — FEI 3007835716

The FDA completed an inspection of Goodman Co., Ltd on April 3, 2025 in Nagoya. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 3, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Nagoya (Japan)

Additional Details

Postmarket Audit Inspections