FDA-Inspected Site

Diazyme Laboratories

4 FDA inspections are on record for Diazyme Laboratories in Poway, United States.

483· Form 483 issued

Poway, United States · Last updated July 10, 2026

Overview

  • 4 FDA inspections are on record.
  • 2 inspections produced a Form 483.
  • The most recent recorded inspection date is 2016-04-20.

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
18 Apr 2016 – 20 Apr 2016Medical Devices & Rad Health483View 483 →
25 Aug 2011Not recorded483View 483 →
11 Jan 2007Not recordedClean
9 Nov 2005Not recordedClean

Observations on record

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

20 Apr 2016
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Sharon I Gundersen

20 Apr 2016
21 CFR 820.184

DHR content

Cited by Sharon I Gundersen

25 Aug 2011
21 CFR 806.20(b)(4)

Justification for not reporting

Cited by Yvette E Guillermo

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 806.20(b)(4)Cited across public-safe Form 483 observations1x
21 CFR 820.100(a)Cited across public-safe Form 483 observations1x
21 CFR 820.184Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind Diazyme Laboratories' 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