Form 483

FairyGene, Inc. Form 483, 2026-01-15

FDA issued a Form 483 to FairyGene, Inc. on 2026-01-15 with 5 public-safe observations.

483· Form 483 issuedHuman Drugs5 observations

FairyGene, Inc. · Bristol, United States · Issued January 15, 2026

Overview

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

Inspectional observations

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

15 Jan 2026
21 CFR 211.100(a)

Absence of Written Procedures

Cited by Christina K Theodorou, Ofuje D Daniyan

15 Jan 2026
21 CFR 211.166(a)

Lack of written stability program

Cited by Christina K Theodorou, Ofuje D Daniyan

15 Jan 2026
21 CFR 211.22(d)

Procedures not in writing, fully followed

Cited by Christina K Theodorou, Ofuje D Daniyan

15 Jan 2026
21 CFR 211.42(b)

Adequate space lacking to prevent mix-ups and contamination

Cited by Christina K Theodorou, Ofuje D Daniyan

15 Jan 2026
21 CFR 211.67(b)

Written procedures not established/followed

Cited by Christina K Theodorou, Ofuje D Daniyan

Inspected site

FIFairyGene, Inc.Bristol, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.100(a)Cited across public-safe Form 483 observations1x
21 CFR 211.166(a)Cited across public-safe Form 483 observations1x
21 CFR 211.22(d)Cited across public-safe Form 483 observations1x
21 CFR 211.42(b)Cited across public-safe Form 483 observations1x
21 CFR 211.67(b)Cited across public-safe Form 483 observations1x

Source document

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Form 483 source document

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Full 483 report

Get the verbatim text of all 5 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