Clear Guide Medical, Inc
FDA inspection history in Baltimore, Maryland, 2019
- 1
- Form 483
Every document, by year
- Form 483
2019: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Baltimore, Maryland.
Cited most
Across all Clear Guide Medical observations on file
- 21 CFR 820.22Quality audit1
- 21 CFR 820.30(e)Design controls1
- 21 CFR 820.50Purchasing controls1
- 21 CFR 820.70(i)Production and process controls1
The complete Clear Guide Medical file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Baltimore, Maryland
One Form 483 · 2019 · 4 observations
Latest: Form 483, Nov 13, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-11-13 | 483 Form 483 | Baltimore, Maryland | 4 | $99 |
Investigators on these documents
FEI number 3011396687 · most recent document Nov 13, 2019
About Clear Guide Medical, Inc
How many FDA Form 483s has Clear Guide Medical, Inc received?
FDA Intel has 1 Form 483 on file for Clear Guide Medical, Inc; the most recent is dated Nov 13, 2019.
When was Clear Guide Medical, Inc last inspected by FDA?
The most recent FDA inspection document on file for Clear Guide Medical, Inc is a Form 483 dated Nov 13, 2019, for the site in Baltimore, Maryland.
What did FDA cite at Clear Guide Medical, Inc?
The regulations cited most in the observations on file for Clear Guide Medical, Inc are 21 CFR 820.22 (Quality audit), 1 time; 21 CFR 820.30(e) (Design controls), 1 time; 21 CFR 820.50 (Purchasing controls), 1 time.