FDA-Inspected Site

Silliker, Inc.

5 FDA inspections are on record for Silliker, Inc. in Cypress, United States.

483· Form 483 issued

Cypress, United States · Last updated July 10, 2026

Overview

  • 5 FDA inspections are on record.
  • 1 inspection produced a Form 483.
  • The most recent recorded inspection date is 2025-06-30.

At a glance

Inspections

5

Form 483s

1

EIRs

0

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
25 Jun 2025 – 30 Jun 2025Human Drugs483View 483 →
6 Mar 2017 – 7 Mar 2017Human DrugsClean
12 Oct 2011Not recordedClean
7 Feb 2011Not recordedClean
20 May 2010Not recordedClean

Observations on record

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

30 Jun 2025
21 CFR 211.160(b)(4)

Calibration - at intervals, written program, remedial action

Cited by Michael Araneta, Ngozi G Offor

30 Jun 2025
21 CFR 211.194(a)(2)

Laboratory Test Method Verification

Cited by Michael Araneta, Ngozi G Offor

30 Jun 2025
21 CFR 211.22(d)

Procedures not in writing, fully followed

Cited by Michael Araneta, Ngozi G Offor

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 211.160(b)(4)Cited across public-safe Form 483 observations1x
21 CFR 211.194(a)(2)Cited across public-safe Form 483 observations1x
21 CFR 211.22(d)Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind Silliker, 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