Form 483

Kavis Pharma LLC Form 483, 2025-04-09

FDA issued a Form 483 to Kavis Pharma LLC on 2025-04-09 with 3 public-safe observations.

483· Form 483 issuedHuman Drugs3 observations

Kavis Pharma LLC · Sugar Land, United States · Issued April 9, 2025

Overview

  • 3 public-safe observations are available for this inspection.
  • 3 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.

9 Apr 2025
21 CFR 211.113(a)

Procedures for non-sterile drug products

Cited by Camerson E Moore

9 Apr 2025
21 CFR 211.68(b)

Backup data not assured as exact and complete

Cited by Camerson E Moore

9 Apr 2025
FDCA 582(b)(4)

Systems in place to comply with verification requirements

Cited by Camerson E Moore

Inspected site

KPKavis Pharma LLCSugar Land, 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 211.68(b)Cited across public-safe Form 483 observations1x
FDCA 582(b)(4)Cited across public-safe Form 483 observations1x

Source document

PDF
PDF available

Form 483 source document

The source document is available to authorized Atlas users.

Full 483 report

Get the verbatim text of all 3 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

Related Form 483s