Fresenius USA Manufacturing, Inc
FDA inspection history in Knoxville, Tennessee, 2020
- 1
- Form 483
Every document, by year
- Form 483
2020: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2020One Form 483, at Knoxville, Tennessee.
Cited most
Across all Fresenius USA Manufacturing observations on file
- 21 CFR 314.81Other postmarketing reports1
The complete Fresenius USA Manufacturing file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Knoxville, Tennessee
One Form 483 · 2020 · 1 observation
Latest: Form 483, Jun 26, 2020 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2020-06-26 | 483 Form 483 | Knoxville, Tennessee | 1 | $99 |
Investigators on these documents
FEI number 3013546115 · most recent document Jun 26, 2020
About Fresenius USA Manufacturing, Inc
How many FDA Form 483s has Fresenius USA Manufacturing, Inc received?
FDA Intel has 1 Form 483 on file for Fresenius USA Manufacturing, Inc; the most recent is dated Jun 26, 2020.
When was Fresenius USA Manufacturing, Inc last inspected by FDA?
The most recent FDA inspection document on file for Fresenius USA Manufacturing, Inc is a Form 483 dated Jun 26, 2020, for the site in Knoxville, Tennessee.
What did FDA cite at Fresenius USA Manufacturing, Inc?
The regulations cited most in the observations on file for Fresenius USA Manufacturing, Inc are 21 CFR 314.81 (Other postmarketing reports), 1 time.