Rolenn Manufacturing Inc

Form 483 issued December 5, 2024 · Riverside, California

Inspection
Dec 3 – Dec 5, 2024
Investigator
Linda Galindo
Observations
4
Pages
3
FEI number
1000160571

In short: On December 5, 2024, FDA issued a Form 483 with 4 observations to Rolenn Manufacturing Inc in Riverside, California (FEI 1000160571) after an inspection that ran Dec 3 – Dec 5, 2024. The investigator was Linda Galindo. Most observations concern production & process controls and cAPA.

At a glance

Production & process controls and capa account for 3 of 4 observations.

Production & process controls2
CAPA1
Management controls1

What FDA observed

Preview: the opening words of each observation
  1. 01

    Procedures for finished device acceptance have…

  2. 02

    A process whose results cannot be fully verified by subsequent inspection and test has not been…

  3. 03

    Procedures for corrective and preventive action have…

  4. 04

    Procedures for training and identifying training needs…

The full 483

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

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This inspection in context

Questions about this 483

What did FDA find at Rolenn Manufacturing Inc?

FDA listed 4 observations on this Form 483, mostly about production & process controls, cAPA and management controls. The opening words of each observation are shown on this page.

Who inspected Rolenn Manufacturing Inc?

Linda Galindo is named on this Form 483, for the inspection of Dec 3 – Dec 5, 2024. Each investigator has a profile showing what they cite most.

When was Rolenn Manufacturing Inc inspected by FDA?

The inspection ran Dec 3 – Dec 5, 2024, and the Form 483 is dated December 5, 2024.

How do I get the full Form 483 for Rolenn Manufacturing Inc?

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