Products by O2, Inc.
FDA inspection history in Fort Lauderdale, Florida, 2023
- 1
- Form 483
Every document, by year
- Form 483
2023: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2023One Form 483, at Fort Lauderdale, Florida.
Cited most
Across all Products by O2 observations on file
- 21 CFR 211.100(a)Written procedures; deviations2
- 21 CFR 211.110(a)Sampling and testing of in-process materials and drug products1
- 21 CFR 211.122(d)Materials examination and usage criteria1
- 21 CFR 211.160(b)General requirements1
- 21 CFR 211.170(b)Reserve samples1
The complete Products by O2 file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Fort Lauderdale, Florida
One Form 483 · 2023 · 11 observations
Latest: Form 483, Oct 23, 2023 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-10-23 | 483 Form 483 | Fort Lauderdale, Florida | 11 | $99 |
Investigators on these documents
FEI number 3005835723 · most recent document Oct 23, 2023
About Products by O2, Inc.
How many FDA Form 483s has Products by O2, Inc. received?
FDA Intel has 1 Form 483 on file for Products by O2, Inc.; the most recent is dated Oct 23, 2023.
When was Products by O2, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Products by O2, Inc. is a Form 483 dated Oct 23, 2023, for the site in Fort Lauderdale, Florida.
What did FDA cite at Products by O2, Inc.?
The regulations cited most in the observations on file for Products by O2, Inc. are 21 CFR 211.100(a) (Written procedures; deviations), 2 times; 21 CFR 211.110(a) (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.122(d) (Materials examination and usage criteria), 1 time.