Liveyon Labs Inc.
FDA inspection history in Yorba Linda, California, 2019
- 1
- Close-out
- 1
- Form 483
Every document, by year
- Close-out
- Form 483
2019: one close-out letter and one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One close-out letter and one Form 483, at Yorba Linda, California.
Cited most
Across all Liveyon Labs observations on file
- 21 CFR 211.113(a)Control of microbiological contamination2
- 21 CFR 1271.50(a)How do I determine whether a donor is eligible?1
- 21 CFR 1271.75(a)(1)How do I screen a donor?1
- 21 CFR 1271.85(b)(2)What donor testing is required for different types of cells and tissues?1
- 21 CFR 121
The complete Liveyon Labs file.
All 2 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Yorba Linda, California
One close-out letter and one Form 483 · 2019 · 9 observations
Latest: Close-out, Dec 5, 2019 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-12-05 | Close-out Close-out letter | Yorba Linda, California | — | $99 |
| 2019-05-23 | 483 Form 483 | Yorba Linda, California | 9 | $99 |
Investigators on these documents
FEI number 3015381220 · most recent document Dec 5, 2019
About Liveyon Labs Inc.
How many FDA Form 483s has Liveyon Labs Inc. received?
FDA Intel has 1 Form 483 on file for Liveyon Labs Inc.; the most recent is dated May 23, 2019.
When was Liveyon Labs Inc. last inspected by FDA?
The most recent FDA inspection document on file for Liveyon Labs Inc. is a Form 483 dated May 23, 2019, for the site in Yorba Linda, California.
What did FDA cite at Liveyon Labs Inc.?
The regulations cited most in the observations on file for Liveyon Labs Inc. are 21 CFR 211.113(a) (Control of microbiological contamination), 2 times; 21 CFR 1271.50(a) (How do I determine whether a donor is eligible?), 1 time; 21 CFR 1271.75(a)(1) (How do I screen a donor?), 1 time.