Form 483

Orthomerica Products, Inc. Form 483, 2013-05-07

FDA issued a Form 483 to Orthomerica Products, Inc. on 2013-05-07 with 6 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health6 observations

Orthomerica Products, Inc. · Orlando, United States · Issued May 7, 2013

Overview

  • 6 public-safe observations are available for this inspection.
  • 6 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.

7 May 2013
21 CFR 820.30(i)

Design changes - Lack of or Inadequate Procedures

Cited by Angela E Glenn

7 May 2013
21 CFR 820.40

Procedures not adequately established or maintained

Cited by Angela E Glenn

7 May 2013
21 CFR 820.50(a)(3)

Acceptable supplier records, inadequate records

Cited by Angela E Glenn

7 May 2013
21 CFR 820.72(b)

Remedial action

Cited by Angela E Glenn

7 May 2013
21 CFR 820.75(a)

Lack of or inadequate process validation

Cited by Angela E Glenn

Inspected site

OPOrthomerica Products, Inc.Orlando, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.30(i)Cited across public-safe Form 483 observations1x
21 CFR 820.40Cited across public-safe Form 483 observations1x
21 CFR 820.50(a)(3)Cited across public-safe Form 483 observations1x
21 CFR 820.72(b)Cited across public-safe Form 483 observations1x
21 CFR 820.75(a)Cited across public-safe Form 483 observations1x
21 CFR 820.90(a)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 6 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