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Zydot Unlimited, Inc FDA Inspection Record

FEI 1643138 · Inspections, Form 483s, warning letters and import refusals

Zydot Unlimited, Inc is an FDA-inspected facility (FEI 1643138) located in Tulsa, OK, US. RegDataLab tracks 4 FDA inspections at this facility.

What FDA found at this site

Latest inspection
Apr 23, 2025: No Action Indicated (NAI)
Inspections on record
4 (1 OAI, 2 VAI, 1 NAI)
Last OAI inspection
Aug 3, 2017
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
2, latest May 6, 2022

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 23, 2025No Action Indicated (NAI)No citations listed
Apr 26, 2022Voluntary Action Indicated (VAI)Batch record - label (21 CFR 111.260(k)(2))
Written procedures - holding; distributing (21 CFR 111.475(b)(1))
Written procedures - product complaint; review, investigate (21 CFR 111.570(b)(1))
Specifications - identity, purity, strength, composition (21 CFR 111.70(e))
and 1 more
Sep 27, 2018Voluntary Action Indicated (VAI)Written procedures - holding; distributing (21 CFR 111.475(b)(1))
Written procedures - product complaint; review, investigate (21 CFR 111.570(b)(1))
Specifications - identity, purity, strength, composition (21 CFR 111.70(e))
Reserve sample -container-closure system (21 CFR 111.83(b)(1))
and 2 more
Aug 3, 2017Official Action Indicated (OAI)Personnel - qualified - general (21 CFR 111.12(a))
Written procedures - pest control (21 CFR 111.16)
Procedures - calibrating instruments (21 CFR 111.25(a))
Procedures - equipment - cleaning, sanitizing (21 CFR 111.25(c))
and 16 more

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
May 6, 2022Class IIF-1271-2022Zydot Ultimate Blend The Original Detox Drink Natural Cherry Flavor 16 fl. oz. (473 ml)… and 2 more products
The ingredient list did not declare the preservatives (potassium sorbate, sodium benzoate) and food coloring (R40) in the product.
Aug 10, 2017Class IIF-3410-2017Zydot Ultimate Blend Detox Drink Natural Tropical Ice Flavor 32 fl. oz. (946 ml) and 16…
Undeclared yellow # 5

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
Zydot Unlimited, Inc
Location
Tulsa, OK (US)
Source
inspections

FDA data resources

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