FDA-Inspected Site

Qapel Medical Inc.

1 FDA inspection is on record for Qapel Medical Inc. in Fremont, United States.

483· Form 483 issued

Fremont, United States · Last updated July 12, 2026

Overview

  • 1 FDA inspection is on record.
  • 1 inspection produced a Form 483.
  • The most recent recorded inspection date is 2024-08-08.

At a glance

Inspections

1

Form 483s

1

EIRs

0

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
29 Jul 2024 – 8 Aug 2024Medical Devices & Rad Health483View 483 →

Observations on record

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

8 Aug 2024
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Jocelyn C Turner, Mary A Millner

8 Aug 2024
21 CFR 820.25(b)

Training - Lack of or inadequate procedures

Cited by Jocelyn C Turner, Mary A Millner

8 Aug 2024
21 CFR 820.30(c)

Design input - documentation

Cited by Jocelyn C Turner, Mary A Millner

8 Aug 2024
21 CFR 820.30(f)

Design verification - Lack of or inadequate procedures

Cited by Jocelyn C Turner, Mary A Millner

8 Aug 2024
21 CFR 820.30(i)

Design changes - Lack of or Inadequate Procedures

Cited by Jocelyn C Turner, Mary A Millner

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 820.198(a)Cited across public-safe Form 483 observations1x
21 CFR 820.25(b)Cited across public-safe Form 483 observations1x
21 CFR 820.30(c)Cited across public-safe Form 483 observations1x
21 CFR 820.30(f)Cited across public-safe Form 483 observations1x
21 CFR 820.30(i)Cited across public-safe Form 483 observations1x
21 CFR 820.40Cited across public-safe Form 483 observations1x
21 CFR 820.50(a)(1)Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind Qapel Medical 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