Form 483

OneBlood, Inc. Form 483, 2010-12-03

FDA issued a Form 483 to OneBlood, Inc. on 2010-12-03 with 2 public-safe observations.

483· Form 483 issued2 observations

OneBlood, Inc. · Ocala, United States · Issued December 3, 2010

Overview

  • 2 public-safe observations are available for this inspection.
  • 2 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.

3 Dec 2010
21 CFR 606.100(b)

Establish, maintain and follow manufacturing SOPs

Cited by Jana L Caylor, Nelson E Venerio

3 Dec 2010
21 CFR 606.170(a)

Adverse Reaction - Investigations

Cited by Jana L Caylor, Nelson E Venerio

Inspected site

OIOneBlood, Inc.Ocala, 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 606.170(a)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 2 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