Form 483

Cellay, Inc Form 483, 2016-02-10

FDA issued a Form 483 to Cellay, Inc on 2016-02-10 with 5 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health5 observations

Cellay, Inc · Cambridge, United States · Issued February 10, 2016

Overview

  • 5 public-safe observations are available for this inspection.
  • 5 structured CFR citations are represented.
  • 2 investigators are tied to this Form 483.

Inspectional observations

Each observation cites the regulation FDA found the firm out of compliance with.

10 Feb 2016
21 CFR 806.10(a)(2)

Report of violation of the Act (see 803.52(e)(9))

Cited by James P Finn, Tamara S Rosbury

10 Feb 2016
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by James P Finn, Tamara S Rosbury

10 Feb 2016
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by James P Finn, Tamara S Rosbury

10 Feb 2016
21 CFR 820.70(i)

Documentation of software validation

Cited by James P Finn, Tamara S Rosbury

10 Feb 2016
21 CFR 820.72(a)

Calibration, Inspection, etc. Procedures Lack of or Inadequ

Cited by James P Finn, Tamara S Rosbury

Inspected site

CICellay, IncCambridge, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 806.10(a)(2)Cited across public-safe Form 483 observations1x
21 CFR 820.100(a)Cited across public-safe Form 483 observations1x
21 CFR 820.198(a)Cited across public-safe Form 483 observations1x
21 CFR 820.70(i)Cited across public-safe Form 483 observations1x
21 CFR 820.72(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