Form 483

Gynex Corporation Form 483, 2020-01-06

FDA issued a Form 483 to Gynex Corporation on 2020-01-06 with 12 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health12 observations

Gynex Corporation · Redmond, United States · Issued January 6, 2020

Overview

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

Inspectional observations

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

6 Jan 2020
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by James A Lane

6 Jan 2020
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by James A Lane

6 Jan 2020
21 CFR 820.198(a)

Complaints

Cited by James A Lane

6 Jan 2020
21 CFR 820.198(a)

Complaints

Cited by James A Lane

6 Jan 2020
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by James A Lane

Inspected site

GCGynex CorporationRedmond, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.198(a)Cited across public-safe Form 483 observations4x
21 CFR 820.100(a)Cited across public-safe Form 483 observations2x
21 CFR 820.50(a)(1)Cited across public-safe Form 483 observations2x
21 CFR 820.72(a)Cited across public-safe Form 483 observations2x
21 CFR 820.90(b)(1)Cited across public-safe Form 483 observations2x

Full 483 report

Get the verbatim text of all 12 observations

The full inspection record, as Atlas holds it, 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