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Form 483

Richard D Guyer, Md/Clin Inv Form 483, 2020-02-10

FDA issued a Form 483 to Richard D Guyer, Md/Clin Inv on 2020-02-10 with 1 public-safe observation.

483· Form 483 issuedMedical Devices & Rad Health1 observation

Richard D Guyer, Md/Clin Inv · Plano, United States · Issued February 10, 2020

Overview

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

Inspectional observations

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

10 Feb 2020
21 CFR 812.100

Investigator non-compliance with agreement/plan/regulations

Cited by Camille D Brown, Marilyn S Babu

Inspected site

RDRichard D Guyer, Md/Clin InvPlano, United States

Inspection team

CDCamille D Brown
MSMarilyn S Babu

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 812.100Cited across public-safe Form 483 observations1x

Source document

PDF
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  • 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