Form 483

Lonza Biologics, Inc. Form 483, 2026-04-16

FDA issued a Form 483 to Lonza Biologics, Inc. on 2026-04-16 with 3 public-safe observations.

483· Form 483 issuedBiologics3 observations

Lonza Biologics, Inc. · Portsmouth, United States · Issued April 16, 2026

Overview

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

16 Apr 2026
21 CFR 211.100(a)

Absence of Written Procedures

Cited by Christian Lynch, Laurel A Beer

16 Apr 2026
21 CFR 211.113(b)

Procedures for sterile drug products

Cited by Christian Lynch, Laurel A Beer

16 Apr 2026
21 CFR 211.142

Written warehousing procedures established/followed

Cited by Christian Lynch, Laurel A Beer

Inspected site

LBLonza Biologics, Inc.Portsmouth, 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 211.113(b)Cited across public-safe Form 483 observations1x
21 CFR 211.142Cited 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 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