FDA-Inspected Site

Veritacor Manufacturing, LLC

2 FDA inspections are on record for Veritacor Manufacturing, LLC in Luling, United States.

Clean· No action indicated

Luling, United States · Last updated July 11, 2026

Overview

  • 2 FDA inspections are on record.
  • 1 inspection produced a Form 483.
  • The most recent recorded inspection date is 2025-02-27.

At a glance

Inspections

2

Form 483s

1

EIRs

0

Last outcome

Clean

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
24 Feb 2025 – 27 Feb 2025Foods & CosmeticsClean
29 Aug 2022 – 1 Sep 2022Foods & Cosmetics483View 483 →

Observations on record

Form 483 observations cited at this site, most recent first.

1 Sep 2022
21 CFR 106.50(f)(1)

In-process material - qualified individual

Cited by Bing Lin

1 Sep 2022
21 CFR 106.50(f)(1)

In-process material - qualified individual

Cited by Bing Lin

1 Sep 2022
21 CFR 106.55(c)

Production aggregate sample - final stage, distribution

Cited by Bing Lin

1 Sep 2022
21 CFR 106.55(c)

Production aggregate sample - final stage, distribution

Cited by Bing Lin

1 Sep 2022
21 CFR 106.91(b)(1)(i)

New infant formula finished product - aggregate test

Cited by Bing Lin

Investigators

FDA investigators tied to this site in the record.

Recurring citations

CFR citation patterns observed across this site's inspections.

CitationWhat it coversCited
21 CFR 106.50(f)(1)Cited across public-safe Form 483 observations3x
21 CFR 106.55(c)Cited across public-safe Form 483 observations3x
21 CFR 106.91(b)(1)(i)Cited across public-safe Form 483 observations3x

Full site report

Get the verbatim findings behind Veritacor Manufacturing, LLC's 1 Form 483

Recurring CFR citations, so your team knows what this site gets cited for.

  • The site's full inspection history, with every Form 483 and its outcome
  • Warning letters and recalls tied to the company behind it
  • Whether recurring CFR citations get closed out or repeat