Form 483

Aurolife Pharma LLC Form 483, 2021-12-07

FDA issued a Form 483 to Aurolife Pharma LLC on 2021-12-07 with 9 public-safe observations.

483· Form 483 issuedHuman Drugs9 observations

Aurolife Pharma LLC · Dayton, United States · Issued December 7, 2021

Overview

  • 9 public-safe observations are available for this inspection.
  • 9 structured CFR citations are represented.
  • 3 investigators are tied to this Form 483.

Inspectional observations

Each observation cites the regulation FDA found the firm out of compliance with.

7 Dec 2021
21 CFR 211.160(b)

Scientifically sound laboratory controls

Cited by David A Oluwo, Ko U Min, Jay B Shah

7 Dec 2021
21 CFR 211.165(e)

Test methods

Cited by David A Oluwo, Ko U Min, Jay B Shah

7 Dec 2021
21 CFR 211.180(e)(1)

Review of representative number of batches

Cited by David A Oluwo, Ko U Min, Jay B Shah

7 Dec 2021
21 CFR 211.192

Investigations of discrepancies, failures

Cited by David A Oluwo, Ko U Min, Jay B Shah

7 Dec 2021
21 CFR 211.22(d)

Procedures not in writing, fully followed

Cited by David A Oluwo, Ko U Min, Jay B Shah

Inspected site

APAurolife Pharma LLCDayton, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.160(b)Cited across public-safe Form 483 observations1x
21 CFR 211.165(e)Cited across public-safe Form 483 observations1x
21 CFR 211.180(e)(1)Cited across public-safe Form 483 observations1x
21 CFR 211.192Cited across public-safe Form 483 observations1x
21 CFR 211.22(d)Cited across public-safe Form 483 observations1x
21 CFR 211.58Cited across public-safe Form 483 observations1x
21 CFR 211.67(a)Cited across public-safe Form 483 observations1x
21 CFR 211.67(b)(3)Cited across public-safe Form 483 observations1x
21 CFR 211.68(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 9 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