FDA-Inspected Site

Vitalconnect Inc.

2 FDA inspections are on record for Vitalconnect Inc. in San Jose, United States.

Clean· No action indicated

San Jose, United States · Last updated July 11, 2026

Overview

  • 2 FDA inspections are on record.
  • 1 inspection produced a Form 483.
  • The most recent recorded inspection date is 2024-02-15.

At a glance

Inspections

2

Form 483s

1

EIRs

0

Last outcome

Clean

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
12 Feb 2024 – 15 Feb 2024Medical Devices & Rad HealthClean
22 Jul 2019 – 25 Jul 2019Medical Devices & Rad Health483View 483 →

Observations on record

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

25 Jul 2019
21 CFR 820.184

DHR - not or inadequately maintained

Cited by Stephen C Smith, Tuan A Nguyen

25 Jul 2019
21 CFR 820.184

DHR - not or inadequately maintained

Cited by Stephen C Smith, Tuan A Nguyen

25 Jul 2019
21 CFR 820.40(a)

Document review, approval documentation

Cited by Stephen C Smith, Tuan A Nguyen

25 Jul 2019
21 CFR 820.40(a)

Document review, approval documentation

Cited by Stephen C Smith, Tuan A Nguyen

25 Jul 2019
21 CFR 820.40(b)

Document change records, maintained.

Cited by Stephen C Smith, Tuan A Nguyen

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 820.184Cited across public-safe Form 483 observations4x
21 CFR 820.40(a)Cited across public-safe Form 483 observations4x
21 CFR 820.40(b)Cited across public-safe Form 483 observations2x

Full site report

Get the verbatim findings behind Vitalconnect Inc.'s 1 Form 483

Verbatim observations 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