Form 483

Mindray DS USA, Inc. dba Mindray North America Form 483, 2015-03-10

FDA issued a Form 483 to Mindray DS USA, Inc. dba Mindray North America on 2015-03-10 with 5 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health5 observations

Mindray DS USA, Inc. dba Mindray North America · Mahwah, United States · Issued March 10, 2015

Overview

  • 5 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.

10 Mar 2015
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by David H Smith

10 Mar 2015
21 CFR 820.72(a)

Equipment suitability & capability

Cited by David H Smith

10 Mar 2015
21 CFR 820.80(d)

Lack of or inadequate final acceptance procedures

Cited by David H Smith

10 Mar 2015
21 CFR 820.86

Acceptance status

Cited by David H Smith

10 Mar 2015
21 CFR 820.90(a)

Nonconforming product control

Cited by David H Smith

Inspected site

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 observations1x
21 CFR 820.72(a)Cited across public-safe Form 483 observations1x
21 CFR 820.80(d)Cited across public-safe Form 483 observations1x
21 CFR 820.86Cited across public-safe Form 483 observations1x
21 CFR 820.90(a)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 5 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