Linatech, Lie
FDA inspection history in Sunnyvale, California, 2019
- 1
- Form 483
Every document, by year
- Form 483
2019: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Sunnyvale, California.
Cited most
Across all Linatech, Lie observations on file
- 21 CFR 820.20(a)Management responsibility4
- 21 CFR 820.198(a)Complaint files2
- 21 CFR 820.100(a)Corrective and preventive action1
- 21 CFR 820.200(a)Servicing1
- 21 CFR 820.40Document controls1
The complete Linatech, Lie file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Sunnyvale, California
One Form 483 · 2019 · 9 observations
Latest: Form 483, Nov 8, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-11-08 | 483 Form 483 | Sunnyvale, California | 9 | $99 |
Investigators on these documents
FEI number 3007037519 · most recent document Nov 8, 2019
About Linatech, Lie
How many FDA Form 483s has Linatech, Lie received?
FDA Intel has 1 Form 483 on file for Linatech, Lie; the most recent is dated Nov 8, 2019.
When was Linatech, Lie last inspected by FDA?
The most recent FDA inspection document on file for Linatech, Lie is a Form 483 dated Nov 8, 2019, for the site in Sunnyvale, California.
What did FDA cite at Linatech, Lie?
The regulations cited most in the observations on file for Linatech, Lie are 21 CFR 820.20(a) (Management responsibility), 4 times; 21 CFR 820.198(a) (Complaint files), 2 times; 21 CFR 820.100(a) (Corrective and preventive action), 1 time.