Form 483

Tetracore, Inc. Form 483, 2009-05-28

FDA issued a Form 483 to Tetracore, Inc. on 2009-05-28 with 4 public-safe observations.

483· Form 483 issued4 observations

Tetracore, Inc. · Rockville, United States · Issued May 28, 2009

Overview

  • 4 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.

28 May 2009
21 CFR 803.17

Lack of Written MDR Procedures

Cited by Tania E Vizcaino

28 May 2009
21 CFR 820.30(b)

Establish the design and development plan

Cited by Tania E Vizcaino

28 May 2009
21 CFR 820.30(e)

Design review procedures - personnel

Cited by Tania E Vizcaino

28 May 2009
21 CFR 820.75(a)

Documentation

Cited by Tania E Vizcaino

Inspected site

TITetracore, Inc.Rockville, 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 observations1x
21 CFR 820.30(b)Cited across public-safe Form 483 observations1x
21 CFR 820.30(e)Cited across public-safe Form 483 observations1x
21 CFR 820.75(a)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 4 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