FDA Inspection 998483 — Ulrich Medical USA Inc

Ulrich Medical USA Inc — FEI 3005532635

The FDA completed an inspection of Ulrich Medical USA Inc on Jan 12, 2017 in Plano, TX. 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
Jan 12, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Plano, TX (United States)

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