Form 483

Brown Precision Inc Form 483, 2018-02-16

FDA issued a Form 483 to Brown Precision Inc on 2018-02-16 with 8 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health8 observations

Brown Precision Inc · Huntsville, United States · Issued February 16, 2018

Overview

  • 8 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.

16 Feb 2018
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Natasha N Mccants

16 Feb 2018
21 CFR 820.90(b)(2)

Product rework procedures, Lack of or inadequate procedures

Cited by Natasha N Mccants

16 Feb 2018
21 CFR 820.90(b)(2)

Product rework procedures, Lack of or inadequate procedures

Cited by Natasha N Mccants

16 Feb 2018
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Natasha N Mccants

16 Feb 2018
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Natasha N Mccants

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 observations2x
21 CFR 820.198(a)Cited across public-safe Form 483 observations2x
21 CFR 820.72(a)Cited across public-safe Form 483 observations2x
21 CFR 820.90(b)(2)Cited across public-safe Form 483 observations2x

Full 483 report

Get the verbatim text of all 8 observations

The full inspection record, as Atlas holds it, 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