Form 483

Lynx Medical Pennsylvania Form 483, 2018-08-17

FDA issued a Form 483 to Lynx Medical Pennsylvania on 2018-08-17 with 12 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health12 observations

Lynx Medical Pennsylvania · Erie, United States · Issued August 17, 2018

Overview

  • 12 public-safe observations are available for this inspection.
  • 6 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.

17 Aug 2018
21 CFR 803.17

Lack of Written MDR Procedures

Cited by Katelyn A Staub-Zamperini

17 Aug 2018
21 CFR 803.17

Lack of Written MDR Procedures

Cited by Katelyn A Staub-Zamperini

17 Aug 2018
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Katelyn A Staub-Zamperini

17 Aug 2018
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Katelyn A Staub-Zamperini

17 Aug 2018
21 CFR 820.198(a)

Complaints

Cited by Katelyn A Staub-Zamperini

Inspected site

LMLynx Medical PennsylvaniaErie, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 803.17Cited across public-safe Form 483 observations2x
21 CFR 820.100(a)Cited across public-safe Form 483 observations2x
21 CFR 820.198(a)Cited across public-safe Form 483 observations2x
21 CFR 820.70(a)Cited across public-safe Form 483 observations2x
21 CFR 820.70(g)(1)Cited across public-safe Form 483 observations2x
21 CFR 820.90(a)Cited across public-safe Form 483 observations2x

Full 483 report

Get the verbatim text of all 12 observations

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