FDA-Inspected Site

Advin Biotech, Inc.

2 FDA inspections are on record for Advin Biotech, Inc. in San Diego, United States.

483· Form 483 issued

San Diego, United States · Last updated August 15, 2026

Overview

  • 2 FDA inspections are on record.
  • 1 inspection produced a Form 483.
  • The most recent recorded inspection date is 2025-09-05.

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
2 Sep 2025 – 5 Sep 2025Medical Devices & Rad Health483View 483 →
16 Jun 2016Medical Devices & Rad HealthClean

Observations on record

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

5 Sep 2025
21 CFR 820.70(h)

Use and removal, Lack of or inadequate procedures

Cited by Juanj Wu

5 Sep 2025
21 CFR 820.70(h)

Use and removal, Lack of or inadequate procedures

Cited by Juanj Wu

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 820.70(h)Cited across public-safe Form 483 observations2x

Full site report

Get the verbatim findings behind Advin Biotech, 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