Form 483

Eli Lilly & Company Form 483, 2010-09-03

FDA issued a Form 483 to Eli Lilly & Company on 2010-09-03 with 2 public-safe observations.

483· Form 483 issued2 observations

Eli Lilly & Company · Indianapolis, United States · Issued September 3, 2010

Overview

  • 2 public-safe observations are available for this inspection.
  • 2 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.

3 Sep 2010
21 CFR 314.80(c)(1)(i)

Late submission of 15-day report

Cited by David A Paterson, Patsy J Domingo

3 Sep 2010
21 CFR 600.80(b)

Review of Adverse Experiences - follow up information

Cited by David A Paterson, Patsy J Domingo

Inspected site

ELEli Lilly & CompanyIndianapolis, United States

Inspection team

PJPatsy J Domingo

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 314.80(c)(1)(i)Cited across public-safe Form 483 observations1x
21 CFR 600.80(b)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 2 observations

The source PDF and 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