Curia New York, Inc.

FDA inspection history across 2 sites, 2004 to 2026

3
Form 483s
1
Warning letter

Every document, by year

  • Warning letter
  • Form 483

2004: one Form 483; 2015: one Form 483; 2023: one Form 483; 2026: one warning letter.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2004One Form 483, at Rensselaer, New York.
  2. 2004The longest 483 on file: 10 observations over 17 pages at Rensselaer, New York.
  3. 2015One Form 483, at Rensselaer, New York.
  4. 2023One Form 483, at Rensselaer, New York.
  5. 2026One warning letter, at Raleigh, North Carolina.

Cited most

Across all Curia New York observations on file

The complete Curia New York file.

All 4 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.

$396

The price of the documents, added to your cart together

Sites

Documents

4 on file, newest first
DateDocumentPrice
2026-09-18Warning letter Warning letter$99
2023-11-01483 Form 483$99
2015-05-22483 Form 483$99
2004-01-01483 Form 483$99

FEI number 1310298 · most recent document Sep 18, 2026

About Curia New York, Inc.

How many FDA Form 483s has Curia New York, Inc. received?

FDA Intel has 3 Form 483s on file for Curia New York, Inc.; the most recent is dated Nov 1, 2023.

When was Curia New York, Inc. last inspected by FDA?

The most recent FDA inspection document on file for Curia New York, Inc. is a Form 483 dated Nov 1, 2023, for the site in Rensselaer, New York.

What did FDA cite at Curia New York, Inc.?

The regulations cited most in the observations on file for Curia New York, Inc. are 21 CFR 211.194 (Laboratory records), 3 times; 21 CFR 211.160 (General requirements), 2 times; 21 CFR 211.192 (Production record review), 2 times.

Has Curia New York, Inc. received an FDA warning letter?

Yes. FDA Intel has 1 FDA warning letter on file for Curia New York, Inc.; the most recent is dated Sep 18, 2026.