Form 483

AltaThera Pharmaceuticals LLC Form 483, 2022-06-17

FDA issued a Form 483 to AltaThera Pharmaceuticals LLC on 2022-06-17 with 4 public-safe observations.

483· Form 483 issuedHuman Drugs4 observations

AltaThera Pharmaceuticals LLC · Chicago, United States · Issued June 17, 2022

Overview

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

17 Jun 2022
21 CFR 314.80(b)

Failure to develop written procedures

Cited by Jeanne J Thai, Yuanyuan Li, Colleen E Burke

17 Jun 2022
21 CFR 314.80(c)(2)

Late submission of annual safety reports

Cited by Jeanne J Thai, Yuanyuan Li, Colleen E Burke

17 Jun 2022
21 CFR 314.80(j)

Failure to maintain records

Cited by Jeanne J Thai, Yuanyuan Li, Colleen E Burke

17 Jun 2022
21 CFR 314.81(b)(2)

Timely submission

Cited by Jeanne J Thai, Yuanyuan Li, Colleen E Burke

Inspected site

APAltaThera Pharmaceuticals LLCChicago, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 314.80(b)Cited across public-safe Form 483 observations1x
21 CFR 314.80(c)(2)Cited across public-safe Form 483 observations1x
21 CFR 314.80(j)Cited across public-safe Form 483 observations1x
21 CFR 314.81(b)(2)Cited across public-safe Form 483 observations1x

Source document

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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