Form 483

Institute for Human Reproduction (IHR) dba Pinnacle Fertility Form 483, 2023-10-25

FDA issued a Form 483 to Institute for Human Reproduction (IHR) dba Pinnacle Fertility on 2023-10-25 with 4 public-safe observations.

483· Form 483 issuedBiologics4 observations

Institute for Human Reproduction (IHR) dba Pinnacle Fertility · Chicago, United States · Issued October 25, 2023

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.

25 Oct 2023
21 CFR 1271.47(a)

Testing, screening, donor eligibility procedures

Cited by Lesley Mae P Lutao

25 Oct 2023
21 CFR 1271.50(b)(1)

Donor screening standards

Cited by Lesley Mae P Lutao

25 Oct 2023
21 CFR 1271.55(b)(1)

Statement re: certified testing lab

Cited by Lesley Mae P Lutao

25 Oct 2023
21 CFR 1271.60(a)

Completion of eligibility determination

Cited by Lesley Mae P Lutao

Inspected site

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 1271.47(a)Cited across public-safe Form 483 observations1x
21 CFR 1271.50(b)(1)Cited across public-safe Form 483 observations1x
21 CFR 1271.55(b)(1)Cited across public-safe Form 483 observations1x
21 CFR 1271.60(a)Cited across public-safe Form 483 observations1x

Source document

PDF
PDF available

Form 483 source document

The source document is available to authorized Atlas users.

Full 483 report

Get the verbatim text of all 4 observations

The source PDF, 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