Form 483

Quest Diagnostics Nichols Institute Form 483, 2019-09-23

FDA issued a Form 483 to Quest Diagnostics Nichols Institute on 2019-09-23 with 8 public-safe observations.

483· Form 483 issuedBiologics8 observations

Quest Diagnostics Nichols Institute · Chantilly, United States · Issued September 23, 2019

Overview

  • 8 public-safe observations are available for this inspection.
  • 2 structured CFR citations are represented.
  • 3 investigators are tied to this Form 483.

Inspectional observations

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

23 Sep 2019
21 CFR 1271.160(b)(1)

Ensuring appropriate core requirements followed

Cited by Shavon L Square, Amanda B Athey, Amanda B Vega

23 Sep 2019
21 CFR 1271.160(b)(1)

Ensuring appropriate core requirements followed

Cited by Shavon L Square, Amanda B Athey, Amanda B Vega

23 Sep 2019
21 CFR 1271.80(c)

Manufacturer instructions not followed

Cited by Shavon L Square, Amanda B Athey, Amanda B Vega

23 Sep 2019
21 CFR 1271.80(c)

Manufacturer instructions not followed

Cited by Shavon L Square, Amanda B Athey, Amanda B Vega

23 Sep 2019
21 CFR 1271.160(b)(1)

Ensuring appropriate core requirements followed

Cited by Shavon L Square, Amanda B Athey, Amanda B Vega

Inspected site

QDQuest Diagnostics Nichols InstituteChantilly, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 1271.160(b)(1)Cited across public-safe Form 483 observations4x
21 CFR 1271.80(c)Cited across public-safe Form 483 observations4x

Source document

PDF
PDF available

Form 483 source document

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Full 483 report

Get the verbatim text of all 8 observations

The source PDF, 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