Form 483

Lonza Biologics, plc Form 483, 2016-06-24

FDA issued a Form 483 to Lonza Biologics, plc on 2016-06-24 with 4 public-safe observations.

483· Form 483 issuedHuman Drugs4 observations

Lonza Biologics, plc · Slough, United Kingdom · Issued June 24, 2016

Overview

  • 4 public-safe observations are available for this inspection.
  • 4 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.

24 Jun 2016
21 CFR 211.113(a)

Procedures for non-sterile drug products

Cited by Lynda L Perry, Ademola O Daramola

24 Jun 2016
21 CFR 211.192

Investigations of discrepancies, failures

Cited by Lynda L Perry, Ademola O Daramola

24 Jun 2016
21 CFR 211.42(c)(10)(iv)

Environmental Monitoring System

Cited by Lynda L Perry, Ademola O Daramola

24 Jun 2016
21 CFR 211.42(c)(10)(v)

Cleaning System

Cited by Lynda L Perry, Ademola O Daramola

Inspected site

LBLonza Biologics, plcSlough, United Kingdom

Inspection team

AOAdemola O Daramola

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 211.192Cited across public-safe Form 483 observations1x
21 CFR 211.42(c)(10)(iv)Cited across public-safe Form 483 observations1x
21 CFR 211.42(c)(10)(v)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 4 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