Unilever Manufacturing (US), Inc.

Form 483 issued March 10, 2020 · Jonesboro, Arkansas

Inspection
Mar 3 – Mar 10, 2020
Investigator
Shatina R. Alridge
Observations
2
Pages
2
FEI number
3006642851

In short: On March 10, 2020, FDA issued a Form 483 with 2 observations to Unilever Manufacturing (US), Inc. in Jonesboro, Arkansas (FEI 3006642851) after an inspection that ran Mar 3 – Mar 10, 2020. The investigator was Shatina R. Alridge. Most observations concern quality system; the most-cited regulation is 21 CFR 211.192 (production record review).

At a glance

2 of 2 observations on this 483 concern quality system.

Quality system2

Most cited: 21 CFR 211.192 (1×) · 211.22(d) (1×)

What FDA observed

Preview: the opening words of each observation
  1. 01

    Written records of investigations into the failure of a batch or any of its components to…

  2. 02

    The responsibilities and procedures applicable to the quality control unit…

The full 483

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This inspection in context

Questions about this 483

What did FDA find at Unilever Manufacturing (US), Inc.?

FDA listed 2 observations on this Form 483, mostly about quality system. The most-cited regulation is 21 CFR 211.192 (production record review). The opening words of each observation are shown on this page.

Who inspected Unilever Manufacturing (US), Inc.?

Shatina R. Alridge is named on this Form 483, for the inspection of Mar 3 – Mar 10, 2020. Each investigator has a profile showing what they cite most.

When was Unilever Manufacturing (US), Inc. inspected by FDA?

The inspection ran Mar 3 – Mar 10, 2020, and the Form 483 is dated March 10, 2020.

How do I get the full Form 483 for Unilever Manufacturing (US), Inc.?

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