FDA-Inspected Site

Nivagen Pharmaceuticals, Inc.

1 FDA inspection is on record for Nivagen Pharmaceuticals, Inc. in Davis, United States.

483· Form 483 issued

Davis, United States · Last updated August 15, 2026

Overview

  • 1 FDA inspection is on record.
  • 1 inspection produced a Form 483.
  • The most recent recorded inspection date is 2024-11-22.

At a glance

Inspections

1

Form 483s

1

EIRs

0

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
19 Nov 2024 – 22 Nov 2024Human Drugs483View 483 →

Observations on record

Form 483 observations cited at this site, most recent first.

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

Investigators

FDA investigators tied to this site in the record.

Recurring citations

CFR citation patterns observed across this site's inspections.

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 site report

Get the verbatim findings behind Nivagen Pharmaceuticals, Inc.'s 1 Form 483

Recurring CFR citations, so your team knows what this site gets cited for.

  • The site's full inspection history, with every Form 483 and its outcome
  • Warning letters and recalls tied to the company behind it
  • Whether recurring CFR citations get closed out or repeat