Form 483

Jubilant Draximage Inc., dba Jubilant Radiopharma Form 483, 2015-04-16

FDA issued a Form 483 to Jubilant Draximage Inc., dba Jubilant Radiopharma on 2015-04-16 with 4 public-safe observations.

483· Form 483 issuedHuman Drugs4 observations

Jubilant Draximage Inc., dba Jubilant Radiopharma · Macon, United States · Issued April 16, 2015

Overview

  • 4 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.

16 Apr 2015
21 CFR 212.20(e)

Written QA procedures established, followed

Cited by Reba A Gates, Jawaid Hamid

16 Apr 2015
21 CFR 212.40(d)

Contamination, mix-ups and deterioration

Cited by Reba A Gates, Jawaid Hamid

16 Apr 2015
21 CFR 212.20(e)

Written QA procedures established, followed

Cited by Reba A Gates, Jawaid Hamid

16 Apr 2015
21 CFR 212.40(d)

Contamination, mix-ups and deterioration

Cited by Reba A Gates, Jawaid Hamid

Inspected site

Inspection team

JHJawaid Hamid

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 212.20(e)Cited across public-safe Form 483 observations2x
21 CFR 212.40(d)Cited across public-safe Form 483 observations2x

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 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