Form 483

Biowave Corporation Form 483, 2026-05-26

FDA issued a Form 483 to Biowave Corporation on 2026-05-26 with 6 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health6 observations

Biowave Corporation · Westport, United States · Issued May 26, 2026

Overview

  • 6 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.

26 May 2026
21 CFR 803.50(a)(2)

Individual Report of Malfunction

Cited by Katarzyna Plona

26 May 2026
21 CFR 803.50(a)(2)

Individual Report of Malfunction

Cited by Katarzyna Plona

26 May 2026
ISO 13485:2016 Clause 6.1(a)

Resources for quality management system have not been determined or provided

Cited by Katarzyna Plona

26 May 2026
ISO 13485:2016 Clause 6.1(a)

Resources for quality management system have not been determined or provided

Cited by Katarzyna Plona

26 May 2026
ISO 13485:2016 Clause 7.4.3

Purchased product verification activities not established or implemented

Cited by Katarzyna Plona

Inspected site

BCBiowave CorporationWestport, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 803.50(a)(2)Cited across public-safe Form 483 observations2x
ISO 13485:2016 Clause 6.1(a)Cited across public-safe Form 483 observations2x
ISO 13485:2016 Clause 7.4.3Cited across public-safe Form 483 observations2x

Full 483 report

Get the verbatim text of all 6 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