Fisher Wallace Laboratories LLC
FDA inspection history in New York, New York, 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 New York, New York.
Cited most
Across all Fisher Wallace Laboratories observations on file
- 21 CFR 803.50(a)(1)If I am a manufacturer, what reporting requirements apply to me?1
- 21 CFR 820.100(b)Corrective and preventive action1
- 21 CFR 820.184Device history record1
- 21 CFR 820.200(a)Servicing1
- 21 CFR 820.80(e)Receiving, in-process, and finished device acceptance1
The complete Fisher Wallace Laboratories file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
New York, New York
One Form 483 · 2016 · 5 observations
Latest: Form 483, Mar 1, 2016 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2016-03-01 | 483 Form 483 | New York, New York | 5 | $99 |
Investigators on these documents
FEI number 3006258094 · most recent document Mar 1, 2016
About Fisher Wallace Laboratories LLC
How many FDA Form 483s has Fisher Wallace Laboratories LLC received?
FDA Intel has 1 Form 483 on file for Fisher Wallace Laboratories LLC; the most recent is dated Mar 1, 2016.
When was Fisher Wallace Laboratories LLC last inspected by FDA?
The most recent FDA inspection document on file for Fisher Wallace Laboratories LLC is a Form 483 dated Mar 1, 2016, for the site in New York, New York.
What did FDA cite at Fisher Wallace Laboratories LLC?
The regulations cited most in the observations on file for Fisher Wallace Laboratories LLC are 21 CFR 803.50(a)(1) (If I am a manufacturer, what reporting requirements apply to me?), 1 time; 21 CFR 820.100(b) (Corrective and preventive action), 1 time; 21 CFR 820.184 (Device history record), 1 time.