Actavis Totowa, LLC
FDA inspection history in Totowa, New Jersey, 2006
- 2
- EIRs
- 1
- Form 483
Every document, by year
- EIR
- Form 483
2006: two inspection reports and one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2006Two inspection reports and one Form 483, at Totowa, New Jersey.
Cited most
Across all Actavis Totowa observations on file
- 21 CFR 211.160General requirements1
- 21 CFR 211.165Testing and release for distribution1
- 21 CFR 211.192Production record review1
- 21 CFR 211.194Laboratory records1
The complete Actavis Totowa file.
All 3 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Totowa, New Jersey
Two inspection reports and one Form 483 · 2006 · 3 observations
Latest: EIR, Nov 30, 2006 →
Documents
3 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2006-11-30 | EIR EIR | Totowa, New Jersey | — | $550 |
| 2006-11-17 | EIR EIR | Totowa, New Jersey | — | $550 |
| 2006-10-11 | 483 Form 483 | Totowa, New Jersey | 3 | $99 |
Investigators on these documents
FEI number 3003450194 · most recent document Nov 30, 2006
About Actavis Totowa, LLC
How many FDA Form 483s has Actavis Totowa, LLC received?
FDA Intel has 1 Form 483 on file for Actavis Totowa, LLC; the most recent is dated Oct 11, 2006.
When was Actavis Totowa, LLC last inspected by FDA?
The most recent FDA inspection document on file for Actavis Totowa, LLC is an establishment inspection report (EIR) dated Nov 30, 2006, for the site in Totowa, New Jersey.
What did FDA cite at Actavis Totowa, LLC?
The regulations cited most in the observations on file for Actavis Totowa, LLC are 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.165 (Testing and release for distribution), 1 time; 21 CFR 211.192 (Production record review), 1 time.