Frostime Llc
FDA inspection history in New York, New York, 2020
- 1
- Form 483
Every document, by year
- Form 483
2020: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2020One Form 483, at New York, New York.
Cited most
Across all Frostime observations on file
- 21 CFR 803.17What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?1
The complete Frostime file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
New York, New York
One Form 483 · 2020 · 1 observation
Latest: Form 483, Oct 28, 2020 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2020-10-28 | 483 Form 483 | New York, New York | 1 | $99 |
Investigators on these documents
FEI number 3016170334 · most recent document Oct 28, 2020
About Frostime Llc
How many FDA Form 483s has Frostime Llc received?
FDA Intel has 1 Form 483 on file for Frostime Llc; the most recent is dated Oct 28, 2020.
When was Frostime Llc last inspected by FDA?
The most recent FDA inspection document on file for Frostime Llc is a Form 483 dated Oct 28, 2020, for the site in New York, New York.
What did FDA cite at Frostime Llc?
The regulations cited most in the observations on file for Frostime Llc are 21 CFR 803.17 (What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?), 1 time.