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Wrist USA (Houston), Inc FDA Inspection Record

FEI 1000117548 · Inspections, Form 483s, warning letters and import refusals

Wrist USA (Houston), Inc is an FDA-inspected facility (FEI 1000117548) located in Pasadena, TX, US. RegDataLab tracks 5 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
Oct 22, 2021: No Action Indicated (NAI)
Inspections on record
5 (1 VAI, 4 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
Oct 22, 2021No Action Indicated (NAI)No citations listed
Jul 11, 2019No Action Indicated (NAI)No citations listed
Apr 10, 2019Voluntary Action Indicated (VAI)No citations listed
Mar 25, 2014No Action Indicated (NAI)No citations listed
Jan 15, 2013No Action Indicated (NAI)No citations listed

Facility details

Company
Wrist USA (Houston), Inc
Location
Pasadena, TX (US)
Source
inspections

FDA data resources

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