FDA Inspection 948561 — Intellijoint Surgical, Inc.

Intellijoint Surgical, Inc. — FEI 3010822102

The FDA completed an inspection of Intellijoint Surgical, Inc. on Oct 29, 2015 in Kitchener. 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
Oct 29, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Kitchener (Canada)

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