NUTCO Inc. Dba Germack Pistachio Co. FDA Inspection Record

FEI 1832009 · Inspections, Form 483s, warning letters and import refusals

NUTCO Inc. Dba Germack Pistachio Co. is an FDA-inspected facility (FEI 1832009) located in Detroit, MI, US. RegDataLab tracks 8 FDA inspections at this facility.

What FDA found at this site

Latest inspection
Apr 14, 2025: No Action Indicated (NAI)
Inspections on record
8 (1 OAI, 4 VAI, 3 NAI)
Last OAI inspection
Mar 3, 2009
Warning letters
None matched to this FEI. Many letters do not state an FEI: search warning letters by company name
Recalls as the recalling firm
5, latest Oct 30, 2017

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 14, 2025No Action Indicated (NAI)Other preventive controls - Record review (21 CFR 117.165(a)(4))
Allergen preventive controls - Implement (21 CFR 117.135(a)(1))
Sanitation preventive controls - Appropriate (Adequate) (21 CFR 117.135(c)(3))
May 9, 2024Voluntary Action Indicated (VAI)Sanitation of non-food-contact surfaces - Manner and frequency (21 CFR 117.35(e))
Supply-chain program - Assurance (Adequate) (21 CFR 117.410(c))
Hazard analysis - Identification of hazard (21 CFR 117.130(a)(1))
Sanitation preventive controls - Appropriate (Adequate) (21 CFR 117.135(c)(3))
Sep 11, 2018Voluntary Action Indicated (VAI)Hazard Analysis - Identification of Hazard (21 CFR 117.130(a)(1))
Preventive Controls - Identify (21 CFR 117.135(a)(1))
Feb 6, 2015Voluntary Action Indicated (VAI)Precautions against contamination--micro, foreign substances (21 CFR 110.10(b)(9))
Materials and workmanship (21 CFR 110.40(a))
Contamination with microorganisms, chemicals, filth, etc. (21 CFR 110.20(b)(2))
Nov 7, 2012No Action Indicated (NAI)No citations listed
Oct 6, 2010Voluntary Action Indicated (VAI)Installation and maintenance of equipment (S) (21 CFR 110.40(a))
Cleaning and sanitizing operations (21 CFR 110.35(a))
Glove condition (21 CFR 110.10(b)(5))
Oct 29, 2009No Action Indicated (NAI)No citations listed
Mar 3, 2009Official Action Indicated (OAI)Buildings/good repair (21 CFR 110.35(a))
Lack of effective pest exclusion (21 CFR 110.35(c))
Failure to clean - general (21 CFR 110.35(d))
Convey sewage (21 CFR 110.37(b)(2))

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
Oct 30, 2017Class IIF-0456-2018Dark Chocolate Almond Bark 5oz &1lb Clear plastic tubs
Germack Roasting is voluntarily recalling its Dark Chocolate Almond Bark following a supplier's recall due to undeclared allergen milk.
Feb 11, 2009Class IF-0515-2010Germack Pistachio Sugar free chocolate peanuts, net wt. 1 lb., Germack Pistachio Co…
The product was manufactured using peanuts recalled by Peanut Corporation of America because they have the potential to be contaminated with…
Jun 9, 2006Class IIF-278-6Germack Pistachio Company Trail Mix - raisins, pineapple, papaya, banana chips, walnuts…
The product contains the undeclared color Yellow #5.
May 25, 2004Class IF-342-4Germack Pistachio Company brand Almonds in 16 oz. bags.
The product was manufactured using almonds that were recalled by Paramount Farms due to their association with an outbreak of Salmonella…
Sep 12, 2003Class IIF-038-4Germack Nut Co. brand Trail Mix in 1 lb. clear bag with a label on the front of the…
The product contains undeclared color, FD&C Yellow #6.

When each source was last refreshed

FDA sources behind this page and when RegDataLab last refreshed each one
RecordsLast refreshedSource as ofStatus
InspectionsNov 14, 2026Newest record Nov 5, 2026Current
Inspection citationsNov 14, 2026Newest record Nov 5, 2026Current
Compliance actions (warning letters, injunctions and other action types)Nov 2, 2026Newest record Oct 29, 2026Current
Warning letter textNov 14, 2026Newest record Nov 10, 2026Current
Recalls (Enforcement Report)Nov 14, 2026Newest record Nov 11, 2026Current
Form 483s and inspection documentsNov 13, 2026Newest record Nov 12, 2026Current
Import refusalsNov 2, 2026Newest record Oct 22, 2026Current

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Facility details

Company
NUTCO Inc.
Location
Detroit, MI (US)
Source
inspections

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