ARCOR SAIC — FDA Facility Profile

FEI 3004383016

ARCOR SAIC is an FDA-inspected facility (FEI 3004383016) located in Villa Mercedes, AR. RegDataLab tracks 3 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
May 9, 2019: No Action Indicated (NAI)
Inspections on record
3 (2 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
Import refusals
1

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
May 9, 2019No Action Indicated (NAI)No citations listed
Nov 1, 2011Voluntary Action Indicated (VAI)Precluding contaminants (21 CFR 110.40(a))
Buildings/good repair (21 CFR 110.35(a))
Lack of effective pest exclusion (21 CFR 110.35(c))
Odor, attractant for pests, harborage (21 CFR 110.37(f))
and 4 more
Jun 17, 2009Voluntary Action Indicated (VAI)No citations listed

Facility details

Company
ARCOR SAIC
Location
Villa Mercedes (AR)
Source
inspections

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