IntelliCell Biosciences, Inc.
FDA inspection history in New York, New York, 2011
- 1
- Form 483
Every document, by year
- Form 483
2011: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2011One Form 483, at New York, New York.
Cited most
Across all IntelliCell Biosciences observations on file
- 21 CFR 211.100Written procedures; deviations3
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.160General requirements1
- 21 CFR 211.165Testing and release for distribution1
- 21 CFR 211.188Batch production and control records1
The complete IntelliCell Biosciences file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
New York, New York
One Form 483 · 2011 · 13 observations
Latest: Form 483, Dec 12, 2011 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2011-12-12 | 483 Form 483 | New York, New York | 13 | $99 |
Investigators on these documents
FEI number 3009237709 · most recent document Dec 12, 2011
About IntelliCell Biosciences, Inc.
How many FDA Form 483s has IntelliCell Biosciences, Inc. received?
FDA Intel has 1 Form 483 on file for IntelliCell Biosciences, Inc.; the most recent is dated Dec 12, 2011.
When was IntelliCell Biosciences, Inc. last inspected by FDA?
The most recent FDA inspection document on file for IntelliCell Biosciences, Inc. is a Form 483 dated Dec 12, 2011, for the site in New York, New York.
What did FDA cite at IntelliCell Biosciences, Inc.?
The regulations cited most in the observations on file for IntelliCell Biosciences, Inc. are 21 CFR 211.100 (Written procedures; deviations), 3 times; 21 CFR 211.113 (Control of microbiological contamination), 1 time; 21 CFR 211.160 (General requirements), 1 time.