FDA Inspection 575291 — Guangzhou Wondfo Biotech Co., Ltd.

Guangzhou Wondfo Biotech Co., Ltd. — FEI 3004635103

The FDA completed an inspection of Guangzhou Wondfo Biotech Co., Ltd. on Mar 27, 2009 in Guangzhou. 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
Mar 27, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Guangzhou (China)

Additional Details

Sponsor, Contract Research Organization

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