Vida Diagnostics, Inc.

FDA Regulatory Profile

Vida Diagnostics, Inc. has 0 FDA recalls, 3 inspections, 2 510(k) clearances and 0 compliance actions on record.

Latest inspection
Oct 3, 2016 · NAI
Latest 510(k)
Aug 7, 2020

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances2Oct 4, 2026Not statedCurrent
Inspections3Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Oct 3, 2016Coralville, IADevicesNo Action Indicated (NAI)3007233544
Jan 14, 2014Coralville, IADevicesNo Action Indicated (NAI)3007233544
Jan 25, 2012Coralville, IADevicesVoluntary Action Indicated (VAI)3007233544

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

Recent 510(k) Clearances

K-NumberDeviceDate
K200990VIDAvisionAug 7, 2020
K083227VIDA PULMONARY WORKSTATION 2 (PW2)Nov 18, 2008