FDA Inspection 1095174 — Shockwave Medical, Inc.

Shockwave Medical, Inc. — FEI 3015053858

The FDA completed an inspection of Shockwave Medical, Inc. on Jun 7, 2019 in Santa Clara, CA. 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
Jun 7, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Santa Clara, CA (United States)

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