Form 483

Cobes Industries (Hefei) Co., Ltd. Form 483, 2011-04-28

FDA issued a Form 483 to Cobes Industries (Hefei) Co., Ltd. on 2011-04-28 with 5 public-safe observations.

483· Form 483 issued5 observations

Cobes Industries (Hefei) Co., Ltd. · Hefei, China · Issued April 28, 2011

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.

28 Apr 2011
21 CFR 820.30(a)

Design control - no procedures

Cited by Michael K Larson

28 Apr 2011
21 CFR 820.70(g)(1)

Maintenance schedule, Lack of or inadequate schedule

Cited by Michael K Larson

28 Apr 2011
21 CFR 820.72(a)

Calibration, Inspection, etc. Procedures Lack of or Inadequ

Cited by Michael K Larson

28 Apr 2011
21 CFR 820.75(a)

Lack of or inadequate process validation

Cited by Michael K Larson

28 Apr 2011
21 CFR 820.250(b)

Sampling plans

Cited by Michael K Larson

Inspected site

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.250(b)Cited across public-safe Form 483 observations1x
21 CFR 820.30(a)Cited across public-safe Form 483 observations1x
21 CFR 820.70(g)(1)Cited across public-safe Form 483 observations1x
21 CFR 820.72(a)Cited across public-safe Form 483 observations1x
21 CFR 820.75(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