Columbia University Fertility Center
FDA inspection history on file, 2024
- 1
- Form 483
Every document, by year
- Form 483
2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2024One Form 483.
Cited most
Across all Columbia University Fertility Center observations on file
- 21 CFR 1271.50(a)How do I determine whether a donor is eligible?2
- 21 CFR 1271.65(b)(2)How do I store an HCT/P from a donor determined to be ineligible, and what uses of the HCT/P are not prohibited?1
- 21 CFR 1271.80(b)What are the general requirements for donor testing?1
- 21 CFR 1271.85(b)(2)What donor testing is required for different types of cells and tissues?1
The complete Columbia University Fertility Center file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-12-20 | 483 Form 483 | — | 5 | $99 |
FEI number 3003972435 · most recent document Dec 20, 2024
About Columbia University Fertility Center
How many FDA Form 483s has Columbia University Fertility Center received?
FDA Intel has 1 Form 483 on file for Columbia University Fertility Center; the most recent is dated Dec 20, 2024.
When was Columbia University Fertility Center last inspected by FDA?
The most recent FDA inspection document on file for Columbia University Fertility Center is a Form 483 dated Dec 20, 2024.
What did FDA cite at Columbia University Fertility Center?
The regulations cited most in the observations on file for Columbia University Fertility Center are 21 CFR 1271.50(a) (How do I determine whether a donor is eligible?), 2 times; 21 CFR 1271.65(b)(2) (How do I store an HCT/P from a donor determined to be ineligible, and what uses of the HCT/P are not prohibited?), 1 time; 21 CFR 1271.80(b) (What are the general requirements for donor testing?), 1 time.