Progressive Laboratories, Inc FDA Inspection Record

FEI 1629365 · Inspections, Form 483s, warning letters and import refusals

Progressive Laboratories, Inc is an FDA-inspected facility (FEI 1629365) located in Irving, TX, US. RegDataLab tracks 8 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
Apr 30, 2025: Voluntary Action Indicated (VAI)
Inspections on record
8 (1 OAI, 4 VAI, 3 NAI)
Last OAI inspection
Jan 29, 2013
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 Feb 23, 2018
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
Apr 30, 2025Voluntary Action Indicated (VAI)Allergen preventive controls - Identify (Written) (21 CFR 117.135(a)(1))
Jun 8, 2022Voluntary Action Indicated (VAI)Specifications - identity, purity, strength, composition (21 CFR 111.70(e))
Material review, disposition, follow-up; investigation (21 CFR 111.140 (b)(3)(ii))
Jun 24, 2019No Action Indicated (NAI)No citations listed
Feb 28, 2018Voluntary Action Indicated (VAI)Equipment - protect from contamination (21 CFR 111.27(a)(3)(v))
Equipment - automated - calibrate, inspect (21 CFR 111.30(c))
Records - document; results (21 CFR 111.325(b)(2)(ii))
Record - product complaint; findings (21 CFR 111.570(b)(2)(ii)(F))
and 1 more
Mar 11, 2015No Action Indicated (NAI)No citations listed
Jan 29, 2013Official Action Indicated (OAI)Component - verify identity, dietary ingredient (21 CFR 111.75(a)(1)(i))
Tests, examinations - scientifically valid (21 CFR 111.75(h))
May 14, 2012No Action Indicated (NAI)Batch record - follow master (21 CFR 111.255(c))
Storage requirements (21 CFR 110.35(b)(2))
Batch record - approved, released, rejected; batch (21 CFR 111.260(l)(3))
Record - product complaint; date received, complainant (21 CFR 111.570(b)(2)(ii)(C))
and 3 more
May 6, 2009Voluntary Action Indicated (VAI)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
Feb 23, 2018Class IF-0912-2018Testosterzone 180 count bottle packaged in an amber plastic bottle with a black cap and 3 more products
Recalled dietary supplements may contain undeclared milk.
Jul 1, 2009Class IF-952-9Advocare Meal Replacement Shake Net Wt 2.08 oz (59g) Chocolate Natural & Artificial… and 1 more product
The product was manufactured using an ingredient recalled by Plainview Milk Products Cooperative because it has the potential to be…

Facility details

Company
Progressive Laboratories, Inc
Location
Irving, TX (US)
Source
inspections

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