Form 483

Hyalynx Inc Form 483, 2014-01-31

FDA issued a Form 483 to Hyalynx Inc on 2014-01-31 with 5 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health5 observations

Hyalynx Inc · Madisonville, United States · Issued January 31, 2014

Overview

  • 5 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.

31 Jan 2014
21 CFR 211.22(a)

Lack of quality control unit

Cited by Cynthia T Cain

31 Jan 2014
21 CFR 211.84(d)(2)

Reports of Analysis (Components)

Cited by Cynthia T Cain

31 Jan 2014
21 CFR 211.165(a)

Testing and release for distribution

Cited by Cynthia T Cain

31 Jan 2014
21 CFR 211.167(a)

Sterility/pyrogens - test methods written, followed

Cited by Cynthia T Cain

31 Jan 2014
21 CFR 211.198(a)

Complaint Handling Procedure

Cited by Cynthia T Cain

Inspected site

HIHyalynx IncMadisonville, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.165(a)Cited across public-safe Form 483 observations1x
21 CFR 211.167(a)Cited across public-safe Form 483 observations1x
21 CFR 211.198(a)Cited across public-safe Form 483 observations1x
21 CFR 211.22(a)Cited across public-safe Form 483 observations1x
21 CFR 211.84(d)(2)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 5 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