Liveyon

FDA inspection history in Yorba Linda, California, 2018 to 2019

2
Form 483s

Every document, by year

  • Form 483

2018: one Form 483; 2019: one Form 483.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2018–19Two Form 483s, at Yorba Linda, California.
  2. 2018The longest 483 on file: 8 observations over 6 pages at Yorba Linda, California.

Cited most

Across all Liveyon observations on file

The complete Liveyon file.

All 2 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.

$198

The price of the documents, added to your cart together

Sites

Documents

2 on file, newest first
DateDocumentPrice
2019-05-23483 Form 483$99
2018-09-21483 Form 483$99

FEI number 3013957857 · most recent document May 23, 2019

About Liveyon

How many FDA Form 483s has Liveyon received?

FDA Intel has 2 Form 483s on file for Liveyon; the most recent is dated May 23, 2019.

When was Liveyon last inspected by FDA?

The most recent FDA inspection document on file for Liveyon is a Form 483 dated May 23, 2019, for the site in Yorba Linda, California.

What did FDA cite at Liveyon?

The regulations cited most in the observations on file for Liveyon are 21 CFR 1271.265(c)(1) (Receipt, predistribution shipment, and distribution of an HCT/P), 2 times; 21 CFR 211.198(a) (Complaint files), 2 times; 21 CFR 1271.200(d) (Equipment), 1 time.