Form 483

Xintec Corp Form 483, 2016-09-13

FDA issued a Form 483 to Xintec Corp on 2016-09-13 with 15 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health15 observations

Xintec Corp · Alameda, United States · Issued September 13, 2016

Overview

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

13 Sep 2016
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Sergio Chavez

13 Sep 2016
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Sergio Chavez

13 Sep 2016
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Sergio Chavez

13 Sep 2016
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Sergio Chavez

13 Sep 2016
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Sergio Chavez

Inspected site

XCXintec CorpAlameda, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.100(a)Cited across public-safe Form 483 observations3x
21 CFR 820.198(a)Cited across public-safe Form 483 observations3x
21 CFR 820.20(b)Cited across public-safe Form 483 observations3x
21 CFR 820.70(c)Cited across public-safe Form 483 observations3x
21 CFR 820.72(b)Cited across public-safe Form 483 observations3x

Full 483 report

Get the verbatim text of all 15 observations

Every observation in full, 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