FORDOZ PHARMA CORPORATION
FDA inspection history in East Windsor, New Jersey, 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 East Windsor, New Jersey.
Cited most
Across all FORDOZ PHARMA observations on file
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.42Design and construction features1
- 21 CFR 211.80General requirements1
The complete FORDOZ PHARMA file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
East Windsor, New Jersey
One Form 483 · 2023 · 4 observations
Latest: Form 483, Mar 17, 2023 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-03-17 | 483 Form 483 | East Windsor, New Jersey | 4 | $99 |
Investigators on these documents
FEI number 3012663162 · most recent document Mar 17, 2023
About FORDOZ PHARMA CORPORATION
How many FDA Form 483s has FORDOZ PHARMA CORPORATION received?
FDA Intel has 1 Form 483 on file for FORDOZ PHARMA CORPORATION; the most recent is dated Mar 17, 2023.
When was FORDOZ PHARMA CORPORATION last inspected by FDA?
The most recent FDA inspection document on file for FORDOZ PHARMA CORPORATION is a Form 483 dated Mar 17, 2023, for the site in East Windsor, New Jersey.
What did FDA cite at FORDOZ PHARMA CORPORATION?
The regulations cited most in the observations on file for FORDOZ PHARMA CORPORATION are 21 CFR 211.113 (Control of microbiological contamination), 1 time; 21 CFR 211.42 (Design and construction features), 1 time; 21 CFR 211.80 (General requirements), 1 time.