FDA Inspection 1269122 — Goodman Co., Ltd

Goodman Co., Ltd — FEI 3007835716

The FDA completed an inspection of Goodman Co., Ltd on Apr 3, 2025 in Nagoya. 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
Apr 3, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Project Evaluation: Devices
Location
Nagoya (Japan)

Additional details

Postmarket Audit Inspections

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