Form 483

Brown Precision Inc Form 483, 2022-09-23

FDA issued a Form 483 to Brown Precision Inc on 2022-09-23 with 6 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health6 observations

Brown Precision Inc · Huntsville, United States · Issued September 23, 2022

Overview

  • 6 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.

23 Sep 2022
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Jamie P Webb

23 Sep 2022
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Jamie P Webb

23 Sep 2022
21 CFR 820.50(a)

Evaluation of suppliers, contractors, etc., requirements

Cited by Jamie P Webb

23 Sep 2022
21 CFR 820.72(a)

Calibration, Inspection, etc. Procedures Lack of or Inadequ

Cited by Jamie P Webb

23 Sep 2022
21 CFR 820.75(b)

Lack/Inad procedure-Monitoring/Control of Validated Proces

Cited by Jamie P Webb

Inspected site

BPBrown Precision IncHuntsville, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.100(a)Cited across public-safe Form 483 observations1x
21 CFR 820.198(a)Cited across public-safe Form 483 observations1x
21 CFR 820.50(a)Cited across public-safe Form 483 observations1x
21 CFR 820.72(a)Cited across public-safe Form 483 observations1x
21 CFR 820.75(b)Cited across public-safe Form 483 observations1x
21 CFR 820.90(a)Cited across public-safe Form 483 observations1x

Source document

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PDF available

Form 483 source document

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Full 483 report

Get the verbatim text of all 6 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