FDA Inspection 969069 — Sonomed, Inc.

Sonomed, Inc. — FEI 2433682

The FDA completed an inspection of Sonomed, Inc. on Apr 15, 2016 in Westbury, NY. 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
Apr 15, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Westbury, NY (United States)

Citations

IDCFRDescription
320321 CFR 820.40(b)Document change records, maintained.