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OMNILIFE USA, Inc. Dba Texas OMNILIFE USA, Inc. — FDA Facility Profile

FEI 3011096836

OMNILIFE USA, Inc. Dba Texas OMNILIFE USA, Inc. is an FDA-inspected facility (FEI 3011096836) located in San Jose, CA, US. RegDataLab tracks 2 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
Apr 28, 2023: Voluntary Action Indicated (VAI)
Inspections on record
2 (1 VAI, 1 NAI)
Last OAI inspection
None on record
Warning letters
None matched to this FEI. Many letters do not state an FEI: search warning letters by company name

A Form 483 lists an inspector's observations. OAI means FDA recommends regulatory and/or administrative action. A warning letter is FDA's formal enforcement notice. No record here does not establish that a site is safe. Check this site on FDA's Data Dashboard.

Inspections and what FDA cited

Newest first. Citations are the inspector observations FDA publishes for the inspection.

DateResultWhat FDA cited
Apr 28, 2023Voluntary Action Indicated (VAI)No citations listed
Sep 8, 2017No Action Indicated (NAI)No citations listed

Facility details

Company
OMNILIFE USA, Inc.
Location
San Jose, CA (US)
Source
inspections

FDA data resources

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