Form 483

SpecGx LLC Form 483, 2025-01-17

FDA issued a Form 483 to SpecGx LLC on 2025-01-17 with 4 public-safe observations.

483· Form 483 issuedHuman Drugs4 observations

SpecGx LLC · Hobart, United States · Issued January 17, 2025

Overview

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

Inspectional observations

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

17 Jan 2025
21 CFR 211.113(a)

Procedures for non-sterile drug products

Cited by Edmund F Mrak, Lori M Newman, Armen H Youssoufian, Paige R Mccoy

17 Jan 2025
21 CFR 211.160(a)

Following/documenting laboratory controls

Cited by Edmund F Mrak, Lori M Newman, Armen H Youssoufian, Paige R Mccoy

17 Jan 2025
21 CFR 211.46(b)

Equipment for Environmental Control

Cited by Edmund F Mrak, Lori M Newman, Armen H Youssoufian, Paige R Mccoy

17 Jan 2025
21 CFR 211.67(a)

Cleaning / Sanitizing / Maintenance

Cited by Edmund F Mrak, Lori M Newman, Armen H Youssoufian, Paige R Mccoy

Inspected site

SLSpecGx LLCHobart, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.113(a)Cited across public-safe Form 483 observations1x
21 CFR 211.160(a)Cited across public-safe Form 483 observations1x
21 CFR 211.46(b)Cited across public-safe Form 483 observations1x
21 CFR 211.67(a)Cited across public-safe Form 483 observations1x

Source document

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PDF available

Form 483 source document

The source document is available to authorized Atlas users.

Full 483 report

Get the verbatim text of all 4 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