Liquipak Corporation

Form 483 issued October 16, 2025 · Alma, Michigan

Inspection
Oct 14 – Oct 16, 2025
Investigator
Melissa M. Steiger
Observations
3
Pages
3
FEI number
1815703

In short: On October 16, 2025, FDA issued a Form 483 with 3 observations to Liquipak Corporation in Alma, Michigan (FEI 1815703) after an inspection that ran Oct 14 – Oct 16, 2025. The investigator was Melissa M. Steiger. Most observations concern facilities & equipment and quality system.

At a glance

2 of 3 observations on this 483 concern facilities & equipment.

Facilities & equipment2
Quality system1

What FDA observed

Preview: the opening words of each observation
  1. 01

    Routine calibration and inspection of electronic equipment is not performed according to a written program designed…

  2. 02

    Written procedures are not established and followed for the cleaning and maintenance of equipment, including utensils…

  3. 03

    Written procedures are not established for evaluations done at least annually and including provisions for a…

The full 483

Plus the full detail behind each one, exactly as FDA wrote it.

Get the full 483

This inspection in context

Questions about this 483

What did FDA find at Liquipak Corporation?

FDA listed 3 observations on this Form 483, mostly about facilities & equipment and quality system. The opening words of each observation are shown on this page.

Who inspected Liquipak Corporation?

Melissa M. Steiger is named on this Form 483, for the inspection of Oct 14 – Oct 16, 2025. Each investigator has a profile showing what they cite most.

When was Liquipak Corporation inspected by FDA?

The inspection ran Oct 14 – Oct 16, 2025, and the Form 483 is dated October 16, 2025.

How do I get the full Form 483 for Liquipak Corporation?

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