Form 483

Nivagen Pharmaceuticals, Inc. Form 483, 2024-11-22

FDA issued a Form 483 to Nivagen Pharmaceuticals, Inc. on 2024-11-22 with 4 public-safe observations.

483· Form 483 issuedHuman Drugs4 observations

Nivagen Pharmaceuticals, Inc. · Davis, United States · Issued November 22, 2024

Overview

  • 4 public-safe observations are available for this inspection.
  • 4 structured CFR citations are represented.
  • 1 investigator is tied to this Form 483.

Inspectional observations

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

22 Nov 2024
21 CFR 211.160(a)

Following/documenting laboratory controls

Cited by Saied A Asbagh

22 Nov 2024
21 CFR 211.160(b)(1)

Samples (various types) representative, identified properly

Cited by Saied A Asbagh

22 Nov 2024
21 CFR 211.160(b)(3)

Acceptance of drug products

Cited by Saied A Asbagh

22 Nov 2024
21 CFR 211.25(a)

Training--operations, GMPs, written procedures

Cited by Saied A Asbagh

Inspected site

NPNivagen Pharmaceuticals, Inc.Davis, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.160(a)Cited across public-safe Form 483 observations1x
21 CFR 211.160(b)(1)Cited across public-safe Form 483 observations1x
21 CFR 211.160(b)(3)Cited across public-safe Form 483 observations1x
21 CFR 211.25(a)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 4 observations

The full inspection record, as Atlas holds it, 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