Form FDA 483 Kite Pharma November 2024
FDA inspection history in Frederi ck, Maryland, 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, at Frederi ck, Maryland.
Cited most
Across all Form FDA 483 Kite Pharma November 2024 observations on file
- 21 CFR 600.80Postmarketing reporting of adverse experiences1
The complete Form FDA 483 Kite Pharma November 2024 file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Frederi ck, Maryland
One Form 483 · 2024 · 1 observation
Latest: Form 483, Nov 1, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-11-01 | 483 Form 483 | Frederi ck, Maryland | 1 | $99 |
Investigators on these documents
About Form FDA 483 Kite Pharma November 2024
How many FDA Form 483s has Form FDA 483 Kite Pharma November 2024 received?
FDA Intel has 1 Form 483 on file for Form FDA 483 Kite Pharma November 2024; the most recent is dated Nov 1, 2024.
When was Form FDA 483 Kite Pharma November 2024 last inspected by FDA?
The most recent FDA inspection document on file for Form FDA 483 Kite Pharma November 2024 is a Form 483 dated Nov 1, 2024, for the site in Frederi ck, Maryland.
What did FDA cite at Form FDA 483 Kite Pharma November 2024?
The regulations cited most in the observations on file for Form FDA 483 Kite Pharma November 2024 are 21 CFR 600.80 (Postmarketing reporting of adverse experiences), 1 time.