FDA-Inspected Site

Invivoscribe Technologies, Inc.

4 FDA inspections are on record for Invivoscribe Technologies, Inc. in San Diego, United States.

483· Form 483 issued

San Diego, United States · Last updated July 9, 2026

Overview

  • 4 FDA inspections are on record.
  • 2 inspections produced a Form 483.
  • The most recent recorded inspection date is 2017-03-06.

At a glance

Inspections

4

Form 483s

2

EIRs

0

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
13 Feb 2017 – 6 Mar 2017Medical Devices & Rad Health483On file
1 Feb 2017 – 6 Feb 2017Medical Devices & Rad HealthClean
15 Sep 2014 – 17 Sep 2014Medical Devices & Rad Health483View 483 →
17 Jun 2008Not recordedClean

Observations on record

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

17 Sep 2014
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Shaquenta Y Perkins

Investigators

FDA investigators tied to this site in the record.

Linda Thai1 insp.
Cntrctmntr Anderson1 insp.

Recurring citations

CFR citation patterns observed across this site's inspections.

CitationWhat it coversCited
21 CFR 820.100(a)Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind Invivoscribe Technologies, Inc.'s 2 Form 483s

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