Form 483

Taylor Healthcare Products, Inc. Form 483, 2026-07-08

FDA issued a Form 483 to Taylor Healthcare Products, Inc. on 2026-07-08 with 3 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health3 observations

Taylor Healthcare Products, Inc. · Spring, United States · Issued July 8, 2026

Overview

  • 3 public-safe observations are available for this inspection.
  • 3 structured CFR citations are represented.
  • 1 investigator is tied to this Form 483.

Inspectional observations

Each observation cites the regulation FDA found the firm out of compliance with.

8 Jul 2026
ISO 13485:2016 Clause 4.1.5

Inadequate monitoring and control over outsourced processes

Cited by Yuliana Hernandez-Magana

8 Jul 2026
ISO 13485:2016 Clause 4.2.1

QMS documentation does not include required documents

Cited by Yuliana Hernandez-Magana

8 Jul 2026
ISO 13485:2016 Clause 8.2.2

Complaint handling procedures lack required elements

Cited by Yuliana Hernandez-Magana

Inspected site

THTaylor Healthcare Products, Inc.Spring, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
ISO 13485:2016 Clause 4.1.5Cited across public-safe Form 483 observations1x
ISO 13485:2016 Clause 4.2.1Cited across public-safe Form 483 observations1x
ISO 13485:2016 Clause 8.2.2Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 3 observations

The full inspection record, as Atlas holds it, so your team sees exactly what was cited and how it was answered.

  • The site's full inspection history around this Form 483
  • Whether these citations escalated to a warning letter
  • The investigators involved and the citations they repeat elsewhere