FDA Inspection 1240536 — Medtronic Xomed, Inc.

Medtronic Xomed, Inc. — FEI 1045254

The FDA completed an inspection of Medtronic Xomed, Inc. on Jun 17, 2024 in Jacksonville, FL. 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). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 17, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Jacksonville, FL (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures