Johns Hopkins Fertility Center
FDA inspection history on file, 2025
- 1
- Form 483
Every document, by year
- Form 483
2025: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2025One Form 483.
Cited most
Across all Johns Hopkins Fertility Center observations on file
- 21 CFR 1271.55What records must accompany an HCT/P after the donor-eligibility determination is complete; and what records must I retain?1
- 21 CFR 1271.75How do I screen a donor?1
The complete Johns Hopkins 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 |
|---|---|---|---|---|
| 2025-08-14 | 483 Form 483 | — | 2 | $99 |
FEI number 3003610950 · most recent document Aug 14, 2025
About Johns Hopkins Fertility Center
How many FDA Form 483s has Johns Hopkins Fertility Center received?
FDA Intel has 1 Form 483 on file for Johns Hopkins Fertility Center; the most recent is dated Aug 14, 2025.
When was Johns Hopkins Fertility Center last inspected by FDA?
The most recent FDA inspection document on file for Johns Hopkins Fertility Center is a Form 483 dated Aug 14, 2025.
What did FDA cite at Johns Hopkins Fertility Center?
The regulations cited most in the observations on file for Johns Hopkins Fertility Center are 21 CFR 1271.55 (What records must accompany an HCT/P after the donor-eligibility determination is complete; and what records must I retain?), 1 time; 21 CFR 1271.75 (How do I screen a donor?), 1 time.