Form 483

Spinalight, Inc. Form 483, 2012-07-19

FDA issued a Form 483 to Spinalight, Inc. on 2012-07-19 with 7 public-safe observations.

483· Form 483 issued7 observations

Spinalight, Inc. · Saint Petersburg, United States · Issued July 19, 2012

Overview

  • 7 public-safe observations are available for this inspection.
  • 7 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.

19 Jul 2012
21 CFR 803.17

Lack of Written MDR Procedures

Cited by Joshua J Silvestri

19 Jul 2012
21 CFR 803.17(a)(2)

Lack of System for Determining MDR Events

Cited by Joshua J Silvestri

19 Jul 2012
21 CFR 820.30(j)

Design history file

Cited by Joshua J Silvestri

19 Jul 2012
21 CFR 820.50

Purchasing controls, Lack of or inadequate procedures

Cited by Joshua J Silvestri

19 Jul 2012
21 CFR 820.80(d)

Lack of or inadequate final acceptance procedures

Cited by Joshua J Silvestri

Inspected site

SISpinalight, Inc.Saint Petersburg, 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 803.17(a)(2)Cited across public-safe Form 483 observations1x
21 CFR 820.181Cited across public-safe Form 483 observations1x
21 CFR 820.198(c)Cited across public-safe Form 483 observations1x
21 CFR 820.30(j)Cited across public-safe Form 483 observations1x
21 CFR 820.50Cited across public-safe Form 483 observations1x
21 CFR 820.80(d)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 7 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