Form 483

Pausch LLC Form 483, 2026-03-23

FDA issued a Form 483 to Pausch LLC on 2026-03-23 with 5 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health5 observations

Pausch LLC · Tinton Falls, United States · Issued March 23, 2026

Overview

  • 5 public-safe observations are available for this inspection.
  • 4 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.

23 Mar 2026
ISO 13485:2016 Clause 4.1.2

Risk-based approach not applied to QMS processes

Cited by William R Chang

23 Mar 2026
ISO 13485:2016 Clause 5.6.1

QMS not reviewed by top management at documented planned intervals

Cited by William R Chang

23 Mar 2026
ISO 13485:2016 Clause 7.4.1

Procedures for purchasing process not documented

Cited by William R Chang

23 Mar 2026
ISO 13485:2016 Clause 7.4.1

Records of supplier (re)evaluation, selection, and monitoring not maintained

Cited by William R Chang

23 Mar 2026
ISO 13485:2016 Clause 8.5.2

Corrective action not taken

Cited by William R Chang

Inspected site

PLPausch LLCTinton Falls, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
ISO 13485:2016 Clause 7.4.1Cited across public-safe Form 483 observations2x
ISO 13485:2016 Clause 4.1.2Cited across public-safe Form 483 observations1x
ISO 13485:2016 Clause 5.6.1Cited across public-safe Form 483 observations1x
ISO 13485:2016 Clause 8.5.2Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 5 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