Form 483

RFI, LLC. Form 483, 2017-09-20

FDA issued a Form 483 to RFI, LLC. on 2017-09-20 with 8 public-safe observations.

483· Form 483 issuedFoods & Cosmetics8 observations

RFI, LLC. · Broomfield, United States · Issued September 20, 2017

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.

20 Sep 2017
21 CFR 111.210(h)(1)

Instructions; specifications; quality

Cited by Laura B Kennedy

20 Sep 2017
21 CFR 111.210(h)(1)

Instructions; specifications; quality

Cited by Laura B Kennedy

20 Sep 2017
21 CFR 111.255(c)

Batch record - each step

Cited by Laura B Kennedy

20 Sep 2017
21 CFR 111.255(c)

Batch record - each step

Cited by Laura B Kennedy

20 Sep 2017
21 CFR 111.260(l)(1)(i)

Batch record - quality control review; monitoring

Cited by Laura B Kennedy

Inspected site

RLRFI, LLC.Broomfield, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 111.210(h)(1)Cited across public-safe Form 483 observations2x
21 CFR 111.255(c)Cited across public-safe Form 483 observations2x
21 CFR 111.260(l)(1)(i)Cited across public-safe Form 483 observations2x
21 CFR 111.455(c)Cited across public-safe Form 483 observations2x

Full 483 report

Get the verbatim text of all 8 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