Form 483

Trutek Corp Form 483, 2026-01-16

FDA issued a Form 483 to Trutek Corp on 2026-01-16 with 7 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health7 observations

Trutek Corp · Bridgewater, United States · Issued January 16, 2026

Overview

  • 7 public-safe observations are available for this inspection.
  • 7 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.

16 Jan 2026
21 CFR 801.20(a)

Label to bear a unique device identifier

Cited by Naakesh N Gomanie

16 Jan 2026
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Naakesh N Gomanie

16 Jan 2026
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Naakesh N Gomanie

16 Jan 2026
21 CFR 820.30(a)

Design control - no procedures

Cited by Naakesh N Gomanie

16 Jan 2026
21 CFR 820.50

Purchasing controls, Lack of or inadequate procedures

Cited by Naakesh N Gomanie

Inspected site

TCTrutek CorpBridgewater, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 801.20(a)Cited across public-safe Form 483 observations1x
21 CFR 820.100(a)Cited across public-safe Form 483 observations1x
21 CFR 820.198(a)Cited across public-safe Form 483 observations1x
21 CFR 820.30(a)Cited across public-safe Form 483 observations1x
21 CFR 820.50Cited across public-safe Form 483 observations1x
21 CFR 820.75(a)Cited across public-safe Form 483 observations1x
21 CFR 830.300(a)Cited 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