Quide! Corporation
FDA inspection history in San Diego, California, 2017
- 1
- Form 483
Every document, by year
- Form 483
2017: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2017One Form 483, at San Diego, California.
Cited most
Across all Quide! observations on file
- 21 CFR 820.40Document controls1
- 21 CFR 820.50Purchasing controls1
- 21 CFR 820.72Inspection, measuring, and test equipment1
- 21 CFR 820.80Receiving, in-process, and finished device acceptance1
The complete Quide! file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
San Diego, California
One Form 483 · 2017 · 4 observations
Latest: Form 483, Apr 10, 2017 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2017-04-10 | 483 Form 483 | San Diego, California | 4 | $99 |
FEI number 2024674 · most recent document Apr 10, 2017
About Quide! Corporation
How many FDA Form 483s has Quide! Corporation received?
FDA Intel has 1 Form 483 on file for Quide! Corporation; the most recent is dated Apr 10, 2017.
When was Quide! Corporation last inspected by FDA?
The most recent FDA inspection document on file for Quide! Corporation is a Form 483 dated Apr 10, 2017, for the site in San Diego, California.
What did FDA cite at Quide! Corporation?
The regulations cited most in the observations on file for Quide! Corporation are 21 CFR 820.40 (Document controls), 1 time; 21 CFR 820.50 (Purchasing controls), 1 time; 21 CFR 820.72 (Inspection, measuring, and test equipment), 1 time.