Form 483

Organogenesis, Inc. Form 483, 2018-06-08

FDA issued a Form 483 to Organogenesis, Inc. on 2018-06-08 with 4 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health4 observations

Organogenesis, Inc. · Canton, United States · Issued June 8, 2018

Overview

  • 4 public-safe observations are available for this inspection.
  • 1 structured CFR citation is represented.
  • 1 investigator is tied to this Form 483.

Inspectional observations

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

8 Jun 2018
21 CFR 820.50(a)

Evaluation of suppliers, contractors, etc., requirements

Cited by Elizabeth B Griffin

8 Jun 2018
21 CFR 820.50(a)

Evaluation of suppliers, contractors, etc., requirements

Cited by Elizabeth B Griffin

8 Jun 2018
21 CFR 820.50(a)

Evaluation of suppliers, contractors, etc., requirements

Cited by Elizabeth B Griffin

8 Jun 2018
21 CFR 820.50(a)

Evaluation of suppliers, contractors, etc., requirements

Cited by Elizabeth B Griffin

Inspected site

OIOrganogenesis, Inc.Canton, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.50(a)Cited across public-safe Form 483 observations4x

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 4 observations

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