Virginia Mason Medical Center
FDA inspection history in Seattle, Washington, 2016
- 1
- Form 483
Every document, by year
- Form 483
2016: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2016One Form 483, at Seattle, Washington.
Cited most
Across all Virginia Mason Medical Center observations on file
- 21 CFR 803.18(b)(1)(i)What are the requirements for establishing and maintaining MDR files or records that apply to me?2
- 21 CFR 803.17What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?1
- 21 CFR 803.30(a)(2)If I am a user facility, what reporting requirements apply to me?1
The complete Virginia Mason Medical Center file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Seattle, Washington
One Form 483 · 2016 · 4 observations
Latest: Form 483, Apr 15, 2016 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2016-04-15 | 483 Form 483 | Seattle, Washington | 4 | $99 |
Investigators on these documents
Christopher S. Genther (1)Sharon I. Gundersen (1)Stephen R. Souza (1)
FEI number 3001239271 · most recent document Apr 15, 2016
About Virginia Mason Medical Center
How many FDA Form 483s has Virginia Mason Medical Center received?
FDA Intel has 1 Form 483 on file for Virginia Mason Medical Center; the most recent is dated Apr 15, 2016.
When was Virginia Mason Medical Center last inspected by FDA?
The most recent FDA inspection document on file for Virginia Mason Medical Center is a Form 483 dated Apr 15, 2016, for the site in Seattle, Washington.
What did FDA cite at Virginia Mason Medical Center?
The regulations cited most in the observations on file for Virginia Mason Medical Center are 21 CFR 803.18(b)(1)(i) (What are the requirements for establishing and maintaining MDR files or records that apply to me?), 2 times; 21 CFR 803.17 (What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?), 1 time; 21 CFR 803.30(a)(2) (If I am a user facility, what reporting requirements apply to me?), 1 time.