LivaNova USA, Inc
FDA inspection history in Houston, Texas, 2021
- 1
- Form 483
Every document, by year
- Form 483
2021: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2021One Form 483, at Houston, Texas.
Cited most
Across all LivaNova USA observations on file
- 21 CFR 820.75(a)Process validation1
The complete LivaNova USA file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Houston, Texas
One Form 483 · 2021 · 1 observation
Latest: Form 483, May 4, 2021 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2021-05-04 | 483 Form 483 | Houston, Texas | 1 | $99 |
Investigators on these documents
FEI number 1000117004 · most recent document May 4, 2021
About LivaNova USA, Inc
How many FDA Form 483s has LivaNova USA, Inc received?
FDA Intel has 1 Form 483 on file for LivaNova USA, Inc; the most recent is dated May 4, 2021.
When was LivaNova USA, Inc last inspected by FDA?
The most recent FDA inspection document on file for LivaNova USA, Inc is a Form 483 dated May 4, 2021, for the site in Houston, Texas.
What did FDA cite at LivaNova USA, Inc?
The regulations cited most in the observations on file for LivaNova USA, Inc are 21 CFR 820.75(a) (Process validation), 1 time.