Form 483

OneBlood, Inc. Form 483, 2013-12-16

FDA issued a Form 483 to OneBlood, Inc. on 2013-12-16 with 4 public-safe observations.

483· Form 483 issuedBiologics4 observations

OneBlood, Inc. · Fort Lauderdale, United States · Issued December 16, 2013

Overview

  • 4 public-safe observations are available for this inspection.
  • 4 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.

16 Dec 2013
21 CFR 606.100(b)

Establish, maintain and follow manufacturing SOPs

Cited by Colleen M Aspinwall

16 Dec 2013
21 CFR 606.100(c)

Thorough investigations

Cited by Colleen M Aspinwall

16 Dec 2013
21 CFR 606.160(a)(1)

Concurrent documentation

Cited by Colleen M Aspinwall

16 Dec 2013
21 CFR 606.171

Biological product deviation report

Cited by Colleen M Aspinwall

Inspected site

OIOneBlood, Inc.Fort Lauderdale, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 606.100(b)Cited across public-safe Form 483 observations1x
21 CFR 606.100(c)Cited across public-safe Form 483 observations1x
21 CFR 606.160(a)(1)Cited across public-safe Form 483 observations1x
21 CFR 606.171Cited 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