Form 483

Regeneron Pharmaceuticals, Inc. Form 483, 2019-10-18

FDA issued a Form 483 to Regeneron Pharmaceuticals, Inc. on 2019-10-18 with 1 public-safe observation.

483· Form 483 issuedHuman Drugs1 observation

Regeneron Pharmaceuticals, Inc. · Rensselaer, United States · Issued October 18, 2019

Overview

  • 1 public-safe observation is available for this inspection.
  • 1 structured CFR citation is represented.
  • 3 investigators are tied to this Form 483.

Inspectional observations

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

18 Oct 2019
21 CFR 211.22(d)

Procedures not in writing, fully followed

Cited by Sony Mathews, Patric C Klotzbuecher, Mindy M Chou

Inspected site

RPRegeneron Pharmaceuticals, Inc.Rensselaer, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.22(d)Cited across public-safe Form 483 observations1x

Source document

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Form 483 source document

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Full 483 report

Get the verbatim text of all 1 observation

The source PDF and every observation in full, 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