Great American Deli, LLC — FDA Facility Profile

FEI 1022617

Great American Deli, LLC is an FDA-inspected facility (FEI 1022617) located in Ooltewah, TN, US. RegDataLab tracks 10 FDA inspections and 1 compliance action at this facility.

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What FDA found at this site

Latest inspection
May 7, 2025: No Action Indicated (NAI)
Inspections on record
10 (1 OAI, 2 VAI, 7 NAI)
Last OAI inspection
Mar 3, 2011
Warning letters
1 listed by FDA for this FEI, latest Jul 22, 2011
Recalls as the recalling firm
3, latest Dec 23, 2019

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 7, 2025No Action Indicated (NAI)No citations listed
May 6, 2022Voluntary Action Indicated (VAI)Critical control points (21 CFR 123.6(c)(2))
Sep 20, 2019No Action Indicated (NAI)Sanitation Controls Procedures (21 CFR 117.135(c)(3))
Apr 6, 2017No Action Indicated (NAI)No citations listed
Jun 18, 2015No Action Indicated (NAI)No citations listed
Nov 21, 2014Voluntary Action Indicated (VAI)Drip and condensate (21 CFR 110.20(b)(4))
Safe and adequate for use (21 CFR 110.35(d)(5))
HACCP plan implementation (21 CFR 123.6(b))
Nov 2, 2011No Action Indicated (NAI)No citations listed
Mar 3, 2011Official Action Indicated (OAI)Non food-contact equipment in processing area (21 CFR 110.40(c))
Floors, walls and ceilings (21 CFR 110.20(b)(4))
Drip and condensate (21 CFR 110.20(b)(4))
Reasonable precautions (21 CFR 110.80)
and 5 more
Jun 3, 2010No Action Indicated (NAI)No citations listed
May 26, 2009No Action Indicated (NAI)No citations listed

Recalls

Newest first. Recalls FDA's Enforcement Report lists with this FEI as the recalling firm. The recalling firm is not always the site that made the product. Search FDA's Enforcement Report by recall number.

DateClassRecallProduct and reason
Dec 23, 2019Class IF-0567-2020Egg Salad Sandwich
Almark Foods issued recall for potential Listeria monocytogenes in ingredient used by firm's supplier.
Oct 6, 2017Class IF-0039-2018GREAT AMERICAN DELI PREMIUM CHICKEN SALAD WHEATBERRRY sandwiches are packaged in a…
Product contains undeclared eggs and soy.
May 12, 2006Class IIF-207-6Tuna Salad on Multi-Grain Bread sandwiches, net wt. 5 oz. under the following labels: a)… and 1 more product
Sandwiches were manufactured using tuna salad which may contain a canned celery ingredient which was inadequately acidified to prevent the…

Facility details

Company
Great American Deli, LLC
Location
Ooltewah, TN (US)
Source
inspections

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