FDA-Inspected Site

Cardiva Medical, Inc.

2 FDA inspections are on record for Cardiva Medical, Inc. in Santa Clara, United States.

483· Form 483 issued

Santa Clara, United States · Last updated July 10, 2026

Overview

  • 2 FDA inspections are on record.
  • 1 inspection produced a Form 483.
  • The most recent recorded inspection date is 2023-07-21.

At a glance

Inspections

2

Form 483s

1

EIRs

0

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
17 Jul 2023 – 21 Jul 2023Medical Devices & Rad Health483View 483 →
7 Mar 2019 – 14 Mar 2019Medical Devices & Rad HealthClean

Observations on record

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

21 Jul 2023
21 CFR 820.100(b)

Documentation

Cited by Jeffrey S Buckser

21 Jul 2023
21 CFR 820.100(b)

Documentation

Cited by Jeffrey S Buckser

21 Jul 2023
21 CFR 820.198(e)

Records of complaint investigation

Cited by Jeffrey S Buckser

21 Jul 2023
21 CFR 820.198(e)

Records of complaint investigation

Cited by Jeffrey S Buckser

21 Jul 2023
21 CFR 820.20(e)

Quality System Procedures

Cited by Jeffrey S Buckser

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 820.100(b)Cited across public-safe Form 483 observations2x
21 CFR 820.198(e)Cited across public-safe Form 483 observations2x
21 CFR 820.20(e)Cited across public-safe Form 483 observations2x
21 CFR 820.25(b)Cited across public-safe Form 483 observations2x

Full site report

Get the verbatim findings behind Cardiva Medical, Inc.'s 1 Form 483

Source PDFs and 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