Form 483

Currie Medical Inc. Form 483, 2026-05-15

FDA issued a Form 483 to Currie Medical Inc. on 2026-05-15 with 7 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health7 observations

Currie Medical Inc. · Norfolk, United States · Issued May 15, 2026

Overview

  • 7 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.

15 May 2026
ISO 13485:2016 Clause 4.1.5

Inadequate monitoring and control over outsourced processes

Cited by Tiki Dixon

15 May 2026
ISO 13485:2016 Clause 7.1

Product realization risk management processes not documented

Cited by Tiki Dixon

15 May 2026
ISO 13485:2016 Clause 7.5.6

Computer software used in production and service provision not validated

Cited by Tiki Dixon

15 May 2026
ISO 13485:2016 Clause 7.5.6

Procedures for validation of processes not documented

Cited by Tiki Dixon

15 May 2026
ISO 13485:2016 Clause 7.6

Procedures for monitoring and measuring equipment requirements not documented

Cited by Tiki Dixon

Inspected site

CMCurrie Medical Inc.Norfolk, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
ISO 13485:2016 Clause 7.5.6Cited across public-safe Form 483 observations4x
ISO 13485:2016 Clause 4.1.5Cited across public-safe Form 483 observations1x
ISO 13485:2016 Clause 7.1Cited across public-safe Form 483 observations1x
ISO 13485:2016 Clause 7.6Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 7 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