Form 483

Titronics Research & Development Co. Form 483, 2019-07-09

FDA issued a Form 483 to Titronics Research & Development Co. on 2019-07-09 with 14 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health14 observations

Titronics Research & Development Co. · Tiffin, United States · Issued July 9, 2019

Overview

  • 14 public-safe observations are available for this inspection.
  • 4 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.

9 Jul 2019
21 CFR 820.184

Lack of or inadequate DHR procedures

Cited by Christina L Bigham

9 Jul 2019
21 CFR 820.184

Lack of or inadequate DHR procedures

Cited by Christina L Bigham

9 Jul 2019
21 CFR 820.40

Procedures not adequately established or maintained

Cited by Christina L Bigham

9 Jul 2019
21 CFR 820.40

Procedures not adequately established or maintained

Cited by Christina L Bigham

9 Jul 2019
21 CFR 820.72(b)

Calibration procedures - content

Cited by Christina L Bigham

Inspected site

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.184Cited across public-safe Form 483 observations4x
21 CFR 820.72(b)Cited across public-safe Form 483 observations4x
21 CFR 820.90(a)Cited across public-safe Form 483 observations4x
21 CFR 820.40Cited across public-safe Form 483 observations2x

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 14 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