Form 483

Dexcom, Inc. Form 483, 2008-12-10

FDA issued a Form 483 to Dexcom, Inc. on 2008-12-10 with 4 public-safe observations.

483· Form 483 issued4 observations

Dexcom, Inc. · San Diego, United States · Issued December 10, 2008

Overview

  • 4 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.

10 Dec 2008
21 CFR 820.30(f)

Design verification - Lack of or inadequate procedures

Cited by Scott K Zika

10 Dec 2008
21 CFR 820.30(g)

Design validation - software validation not performed

Cited by Scott K Zika

10 Dec 2008
21 CFR 820.70(c)

Environmental control Lack of or inadequate procedures

Cited by Scott K Zika

10 Dec 2008
21 CFR 820.70(c)

Environmental control system periodic inspections

Cited by Scott K Zika

Inspected site

DIDexcom, Inc.San Diego, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.70(c)Cited across public-safe Form 483 observations2x
21 CFR 820.30(f)Cited across public-safe Form 483 observations1x
21 CFR 820.30(g)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 4 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