Clear Image Device LLC
FDA inspection history in Ann Arbor, Michigan, 2015
- 1
- Form 483
Every document, by year
- Form 483
2015: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2015One Form 483, at Ann Arbor, Michigan.
Cited most
Across all Clear Image Device observations on file
- 21 CFR 820.184Device history record2
- 21 CFR 803.17What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?1
- 21 CFR 820.22Quality audit1
- 21 CFR 820.30Design controls1
- 21 CFR 820.50Purchasing controls1
The complete Clear Image Device file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Ann Arbor, Michigan
One Form 483 · 2015 · 6 observations
Latest: Form 483, Aug 20, 2015 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2015-08-20 | 483 Form 483 | Ann Arbor, Michigan | 6 | $99 |
Investigators on these documents
FEI number 3009884681 · most recent document Aug 20, 2015
About Clear Image Device LLC
How many FDA Form 483s has Clear Image Device LLC received?
FDA Intel has 1 Form 483 on file for Clear Image Device LLC; the most recent is dated Aug 20, 2015.
When was Clear Image Device LLC last inspected by FDA?
The most recent FDA inspection document on file for Clear Image Device LLC is a Form 483 dated Aug 20, 2015, for the site in Ann Arbor, Michigan.
What did FDA cite at Clear Image Device LLC?
The regulations cited most in the observations on file for Clear Image Device LLC are 21 CFR 820.184 (Device history record), 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 820.22 (Quality audit), 1 time.