Medscience Inc
FDA inspection history in Delray Beach, Florida, 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 Delray Beach, Florida.
Cited most
Across all Medscience observations on file
- 21 CFR 803.17What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?1
- 21 CFR 820.100(a)Corrective and preventive action1
- 21 CFR 820.160(a)Distribution1
- 21 CFR 820.180General requirements1
- 21 CFR 820.181Device master record1
The complete Medscience file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Delray Beach, Florida
One Form 483 · 2016 · 11 observations
Latest: Form 483, Mar 29, 2016 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2016-03-29 | 483 Form 483 | Delray Beach, Florida | 11 | $99 |
Investigators on these documents
FEI number 3010131789 · most recent document Mar 29, 2016
About Medscience Inc
How many FDA Form 483s has Medscience Inc received?
FDA Intel has 1 Form 483 on file for Medscience Inc; the most recent is dated Mar 29, 2016.
When was Medscience Inc last inspected by FDA?
The most recent FDA inspection document on file for Medscience Inc is a Form 483 dated Mar 29, 2016, for the site in Delray Beach, Florida.
What did FDA cite at Medscience Inc?
The regulations cited most in the observations on file for Medscience Inc are 21 CFR 803.17 (What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?), 1 time; 21 CFR 820.100(a) (Corrective and preventive action), 1 time; 21 CFR 820.160(a) (Distribution), 1 time.