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American Homepatient Inc FDA Inspection Record

FEI 1938040 · Inspections, Form 483s, warning letters and import refusals

American Homepatient Inc is an FDA-inspected facility (FEI 1938040) located in Crystal City, MO, US. RegDataLab tracks 2 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
Aug 10, 2011: Voluntary Action Indicated (VAI)
Inspections on record
2 (2 VAI)
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
Aug 10, 2011Voluntary Action Indicated (VAI)No citations listed
May 27, 2010Voluntary Action Indicated (VAI)Approve or reject procedures or specs (21 CFR 211.22(c))
SOPs not followed / documented (21 CFR 211.100(b))

Facility details

Company
American Homepatient Inc
Location
Crystal City, MO (US)
Source
inspections

FDA data resources

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