FEI 3008189622
FDA inspection history in Tuckahoe, 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 Tuckahoe, New York.
Cited most
Across all site observations on file
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 211.110(a)Sampling and testing of in-process materials and drug products1
- 21 CFR 211.122(e)Materials examination and usage criteria1
- 21 CFR 211.130(c)Packaging and labeling operations1
- 21 CFR 211.160(b)General requirements1
The complete site file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Tuckahoe, New York
One Form 483 · 2016 · 13 observations
Latest: Form 483, Dec 21, 2016 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2016-12-21 | 483 Form 483 | Tuckahoe, New York | 13 | $99 |
Investigators on these documents
FEI number 3008189622 · most recent document Dec 21, 2016
About FEI 3008189622
How many FDA Form 483s has FEI 3008189622 received?
FDA Intel has 1 Form 483 on file for FEI 3008189622; the most recent is dated Dec 21, 2016.
When was FEI 3008189622 last inspected by FDA?
The most recent FDA inspection document on file for FEI 3008189622 is a Form 483 dated Dec 21, 2016, for the site in Tuckahoe, New York.
What did FDA cite at FEI 3008189622?
The regulations cited most in the observations on file for FEI 3008189622 are 21 CFR 211.100(a) (Written procedures; deviations), 1 time; 21 CFR 211.110(a) (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.122(e) (Materials examination and usage criteria), 1 time.