FDA Inspection 1012560 — Saint-Gobain Life Sciences (Hangzhou) Co., Ltd

Saint-Gobain Life Sciences (Hangzhou) Co., Ltd — FEI 3008157119

The FDA completed an inspection of Saint-Gobain Life Sciences (Hangzhou) Co., Ltd on May 11, 2017 in Hangzhou. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
May 11, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Hangzhou (China)

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