FDA-Inspected Site

ZivaQ Pharmaceuticals Inc.

1 FDA inspection is on record for ZivaQ Pharmaceuticals Inc. in East Brunswick, United States.

483· Form 483 issued

East Brunswick, United States · Last updated July 12, 2026

Overview

  • 1 FDA inspection is on record.
  • 1 inspection produced a Form 483.
  • The most recent recorded inspection date is 2026-03-30.

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
16 Mar 2026 – 30 Mar 2026Foods & Cosmetics483View 483 →

Observations on record

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

30 Mar 2026
21 CFR 111.123(b)(3)

Quality control - batch released, adulteration

Cited by James R Birkenstamm, Dhaval H Patel

30 Mar 2026
21 CFR 111.205(b)(2)

Master manufacturing record - controls, procedures

Cited by James R Birkenstamm, Dhaval H Patel

30 Mar 2026
21 CFR 111.20(c)

Physical plant - proper precautions to prevent mix-ups, contamination

Cited by James R Birkenstamm, Dhaval H Patel

30 Mar 2026
21 CFR 111.35(b)

Make and keep records - equipment and utensils

Cited by James R Birkenstamm, Dhaval H Patel

30 Mar 2026
21 CFR 111.75(a)(1)(i)

Component - verify identity, dietary ingredient

Cited by James R Birkenstamm, Dhaval H Patel

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 111.123(b)(3)Cited across public-safe Form 483 observations1x
21 CFR 111.20(c)Cited across public-safe Form 483 observations1x
21 CFR 111.205(b)(2)Cited across public-safe Form 483 observations1x
21 CFR 111.35(b)Cited across public-safe Form 483 observations1x
21 CFR 111.75(a)(1)(i)Cited across public-safe Form 483 observations1x
21 CFR 111.83(b)Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind ZivaQ 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