Form 483

Manhattan Reproductive Medicine, PC Form 483, 2014-09-18

FDA issued a Form 483 to Manhattan Reproductive Medicine, PC on 2014-09-18 with 5 public-safe observations.

483· Form 483 issuedBiologics5 observations

Manhattan Reproductive Medicine, PC · New York, United States · Issued September 18, 2014

Overview

  • 5 public-safe observations are available for this inspection.
  • 5 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.

18 Sep 2014
21 CFR 1271.50(a)

Responsible person to determine, document

Cited by Irina Gaberman

18 Sep 2014
21 CFR 1271.55(d)(2)

Accurate, indelible, legible

Cited by Irina Gaberman

18 Sep 2014
21 CFR 1271.75(a)(1)

Risk factors, clinical evidence

Cited by Irina Gaberman

18 Sep 2014
21 CFR 1271.75(a)(2)

Risks associated with xenotransplantation

Cited by Irina Gaberman

18 Sep 2014
21 CFR 1271.80(c)

Kits not FDA approved, specifically labeled

Cited by Irina Gaberman

Inspected site

MRManhattan Reproductive Medicine, PCNew York, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 1271.50(a)Cited across public-safe Form 483 observations1x
21 CFR 1271.55(d)(2)Cited across public-safe Form 483 observations1x
21 CFR 1271.75(a)(1)Cited across public-safe Form 483 observations1x
21 CFR 1271.75(a)(2)Cited across public-safe Form 483 observations1x
21 CFR 1271.80(c)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 5 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