Cascadia Manufacturing, Inc. d.b.a
FDA inspection history in Bellevue, 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 Bellevue, Washington.
Cited most
Across all Cascadia Manufacturing, Inc. d.b.a observations on file
- 21 CFR 211.160(a)General requirements2
- 21 CFR 211.170(a)Reserve samples2
- 21 CFR 211.84(d)(2)Testing and approval or rejection of components, drug product containers, and closures2
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 211.113(a)Control of microbiological contamination1
The complete Cascadia Manufacturing, Inc. d.b.a file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Bellevue, Washington
One Form 483 · 2016 · 20 observations
Latest: Form 483, Mar 1, 2016 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2016-03-01 | 483 Form 483 | Bellevue, Washington | 20 | $99 |
Investigators on these documents
FEI number 3005105463 · most recent document Mar 1, 2016
About Cascadia Manufacturing, Inc. d.b.a
How many FDA Form 483s has Cascadia Manufacturing, Inc. d.b.a received?
FDA Intel has 1 Form 483 on file for Cascadia Manufacturing, Inc. d.b.a; the most recent is dated Mar 1, 2016.
When was Cascadia Manufacturing, Inc. d.b.a last inspected by FDA?
The most recent FDA inspection document on file for Cascadia Manufacturing, Inc. d.b.a is a Form 483 dated Mar 1, 2016, for the site in Bellevue, Washington.
What did FDA cite at Cascadia Manufacturing, Inc. d.b.a?
The regulations cited most in the observations on file for Cascadia Manufacturing, Inc. d.b.a are 21 CFR 211.160(a) (General requirements), 2 times; 21 CFR 211.170(a) (Reserve samples), 2 times; 21 CFR 211.84(d)(2) (Testing and approval or rejection of components, drug product containers, and closures), 2 times.