Form 483

First Source, Inc. Form 483, 2016-06-10

FDA issued a Form 483 to First Source, Inc. on 2016-06-10 with 5 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health5 observations

First Source, Inc. · Rochester, United States · Issued June 10, 2016

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 Jun 2016
21 CFR 803.17

Lack of Written MDR Procedures

Cited by Gamal A Norton

10 Jun 2016
21 CFR 820.20(c)

Management review - defined interval, sufficient frequency

Cited by Gamal A Norton

10 Jun 2016
21 CFR 820.22

Quality Audit/Reaudit - conducted

Cited by Gamal A Norton

10 Jun 2016
21 CFR 820.50(b)

Supplier notification of changes

Cited by Gamal A Norton

10 Jun 2016
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Gamal A Norton

Inspected site

FSFirst Source, Inc.Rochester, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 803.17Cited across public-safe Form 483 observations1x
21 CFR 820.198(a)Cited across public-safe Form 483 observations1x
21 CFR 820.20(c)Cited across public-safe Form 483 observations1x
21 CFR 820.22Cited across public-safe Form 483 observations1x
21 CFR 820.50(b)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