Advanced Monitored Caregiving
FDA inspection history in New York, New York, 2018 to 2020
- 2
- Form 483s
Every document, by year
- Form 483
2018: one Form 483; 2020: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2018–20Two Form 483s, at New York, New York.
- 2018The longest 483 on file: 4 observations over 4 pages at New York, New York.
Cited most
Across all Advanced Monitored Caregiving observations on file
- 21 CFR 820.80(d)Receiving, in-process, and finished device acceptance2
- 21 CFR 803.17What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?1
- 21 CFR 820.30(i)Design controls1
- 21 CFR 820.50(a)(1)Purchasing controls1
The complete Advanced Monitored Caregiving file.
All 2 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
New York, New York
Two Form 483s · 2018 to 2020 · 5 observations
Latest: Form 483, Nov 12, 2020 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2020-11-12 | 483 Form 483 | New York, New York | 1 | $99 |
| 2018-03-29 | 483 Form 483 | New York, New York | 4 | $99 |
Investigators on these documents
FEI number 3005439460 · most recent document Nov 12, 2020
About Advanced Monitored Caregiving
How many FDA Form 483s has Advanced Monitored Caregiving received?
FDA Intel has 2 Form 483s on file for Advanced Monitored Caregiving; the most recent is dated Nov 12, 2020.
When was Advanced Monitored Caregiving last inspected by FDA?
The most recent FDA inspection document on file for Advanced Monitored Caregiving is a Form 483 dated Nov 12, 2020, for the site in New York, New York.
What did FDA cite at Advanced Monitored Caregiving?
The regulations cited most in the observations on file for Advanced Monitored Caregiving are 21 CFR 820.80(d) (Receiving, in-process, and finished device acceptance), 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 820.30(i) (Design controls), 1 time.