Marietta Corporation
FDA inspection history in Cortland, New York, 2008 to 2015
- 1
- Form 483
- 1
- EIR
Every document, by year
- Form 483
- EIR
2008: one inspection report; 2015: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2008One inspection report, at Cortland, New York.
- 2015One Form 483, at Cortland, New York.
Cited most
Across all Marietta observations on file
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 211.166(a)Stability testing1
- 21 CFR 211.180(e)(1)General requirements1
- 21 CFR 211.192Production record review1
The complete Marietta file.
All 2 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
Cortland, New York
One Form 483 and one inspection report · 2008 to 2015 · 4 observations
Latest: Form 483, Jun 15, 2015 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2015-06-15 | 483 Form 483 | Cortland, New York | 4 | $99 |
| 2008-08-19 | EIR EIR | Cortland, New York | — | $550 |
Investigators on these documents
FEI number 1317302 · most recent document Jun 15, 2015
About Marietta Corporation
How many FDA Form 483s has Marietta Corporation received?
FDA Intel has 1 Form 483 on file for Marietta Corporation; the most recent is dated Jun 15, 2015.
When was Marietta Corporation last inspected by FDA?
The most recent FDA inspection document on file for Marietta Corporation is a Form 483 dated Jun 15, 2015, for the site in Cortland, New York.
What did FDA cite at Marietta Corporation?
The regulations cited most in the observations on file for Marietta Corporation are 21 CFR 211.100(a) (Written procedures; deviations), 1 time; 21 CFR 211.166(a) (Stability testing), 1 time; 21 CFR 211.180(e)(1) (General requirements), 1 time.