Rain Shadow Labs
FDA inspection history in Saint Helens, Oregon, 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 Saint Helens, Oregon.
Cited most
Across all Rain Shadow Labs observations on file
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 211.125(f)Labeling issuance1
- 21 CFR 211.150(b)Distribution procedures1
- 21 CFR 211.160(b)General requirements1
- 21 CFR 211.165(b)Testing and release for distribution1
The complete Rain Shadow Labs file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Saint Helens, Oregon
One Form 483 · 2016 · 11 observations
Latest: Form 483, Mar 22, 2016 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2016-03-22 | 483 Form 483 | Saint Helens, Oregon | 11 | $99 |
Investigators on these documents
FEI number 3006078557 · most recent document Mar 22, 2016
About Rain Shadow Labs
How many FDA Form 483s has Rain Shadow Labs received?
FDA Intel has 1 Form 483 on file for Rain Shadow Labs; the most recent is dated Mar 22, 2016.
When was Rain Shadow Labs last inspected by FDA?
The most recent FDA inspection document on file for Rain Shadow Labs is a Form 483 dated Mar 22, 2016, for the site in Saint Helens, Oregon.
What did FDA cite at Rain Shadow Labs?
The regulations cited most in the observations on file for Rain Shadow Labs are 21 CFR 211.100(a) (Written procedures; deviations), 1 time; 21 CFR 211.125(f) (Labeling issuance), 1 time; 21 CFR 211.150(b) (Distribution procedures), 1 time.