Home / Companies / Avazzia, Inc.

Avazzia, Inc.

FDA Regulatory Profile

Avazzia, Inc. has 0 FDA recalls, 2 inspections, 4 510(k) clearances and 0 compliance actions on record.

Latest inspection
Aug 30, 2017 · NAI
Latest 510(k)
Apr 27, 2021

Reviewing Avazzia, Inc. as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.

Request a free FDA snapshot

Or get Avazzia, Inc.'s full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site, in Claude, Cursor or ChatGPT.

Get a free API key

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances4Oct 4, 2026Not statedCurrent
Inspections2Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Aug 30, 2017Dallas, TXDevicesNo Action Indicated (NAI)3004839404
Jul 13, 2010Dallas, TXDevicesNo Action Indicated (NAI)3004839404

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
K191951Avazzia OTC TENS for aesthetics, model BEST-AV1™: EZZI-LIFT™ DeviceApr 27, 2021
K162392AvazziaMay 12, 2017
K123099Best-AV2 Pro-Sport(tm)May 23, 2014
K062641BODY-STIM, BIOMODULATOR, BEST-RSI, BEST PRO, MODEL BEST-AV1Apr 30, 2007

FDA data resources