Form 483

MPP PHARMA LLC Form 483, 2024-09-20

FDA issued a Form 483 to MPP PHARMA LLC on 2024-09-20 with 2 public-safe observations.

483· Form 483 issuedHuman Drugs2 observations

MPP PHARMA LLC · Kansas City, United States · Issued September 20, 2024

Overview

  • 2 public-safe observations are available for this inspection.
  • 2 structured CFR citations are represented.
  • 2 investigators are tied to this Form 483.

Inspectional observations

Each observation cites the regulation FDA found the firm out of compliance with.

20 Sep 2024
21 CFR 314.80(b)

Failure to develop written procedures

Cited by Jonathan R Campos, Carmen Y Fisher

20 Sep 2024
21 CFR 314.80(c)(1)(i)

Late submission of 15-day report

Cited by Jonathan R Campos, Carmen Y Fisher

Inspected site

MPMPP PHARMA LLCKansas City, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 314.80(b)Cited across public-safe Form 483 observations1x
21 CFR 314.80(c)(1)(i)Cited across public-safe Form 483 observations1x

Source document

PDF
PDF available

Form 483 source document

The source document is available to authorized Atlas users.

Full 483 report

Get the verbatim text of all 2 observations

The source PDF, so your team sees exactly what was cited and how it was answered.

  • The site's full inspection history around this Form 483
  • Whether these citations escalated to a warning letter
  • The investigators involved and the citations they repeat elsewhere