FDA Form 483 Roslin Cell Therapies Limited January 2025
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 FDA Form 483 Roslin Cell Therapies Limited January 2025 observations on file
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.22Responsibilities of quality control unit1
- 21 CFR 211.68Automatic, mechanical, and electronic equipment1
The complete FDA Form 483 Roslin Cell Therapies Limited January 2025 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 |
|---|---|---|---|---|
| 2025-01-21 | 483 Form 483 | — | — | $99 |
About FDA Form 483 Roslin Cell Therapies Limited January 2025
How many FDA Form 483s has FDA Form 483 Roslin Cell Therapies Limited January 2025 received?
FDA Intel has 1 Form 483 on file for FDA Form 483 Roslin Cell Therapies Limited January 2025; the most recent is dated Jan 21, 2025.
When was FDA Form 483 Roslin Cell Therapies Limited January 2025 last inspected by FDA?
The most recent FDA inspection document on file for FDA Form 483 Roslin Cell Therapies Limited January 2025 is a Form 483 dated Jan 21, 2025.
What did FDA cite at FDA Form 483 Roslin Cell Therapies Limited January 2025?
The regulations cited most in the observations on file for FDA Form 483 Roslin Cell Therapies Limited January 2025 are 21 CFR 211.113 (Control of microbiological contamination), 1 time; 21 CFR 211.22 (Responsibilities of quality control unit), 1 time; 21 CFR 211.68 (Automatic, mechanical, and electronic equipment), 1 time.