FinVector Oy
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 FinVector Oy observations on file
- 21 CFR 211.84Testing and approval or rejection of components, drug product containers, and closures2
- 21 CFR 211.110Sampling and testing of in-process materials and drug products1
- 21 CFR 211.22(c)Responsibilities of quality control unit1
- 21 CFR 211.67(b)Equipment cleaning and maintenance1
The complete FinVector Oy 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 |
|---|---|---|---|---|
| 2024-05-28 | 483 Form 483 | — | 5 | $99 |
Investigators on these documents
FEI number 3010227150 · most recent document May 28, 2024
About FinVector Oy
How many FDA Form 483s has FinVector Oy received?
FDA Intel has 1 Form 483 on file for FinVector Oy; the most recent is dated May 28, 2024.
When was FinVector Oy last inspected by FDA?
The most recent FDA inspection document on file for FinVector Oy is a Form 483 dated May 28, 2024.
What did FDA cite at FinVector Oy?
The regulations cited most in the observations on file for FinVector Oy are 21 CFR 211.84 (Testing and approval or rejection of components, drug product containers, and closures), 2 times; 21 CFR 211.110 (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.22(c) (Responsibilities of quality control unit), 1 time.