Curia Massachusetts, Inc.
FDA inspection history in Burlington, Massachusetts, 2017
- 1
- Form 483
Every document, by year
- Form 483
2017: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2017One Form 483, at Burlington, Massachusetts.
Cited most
Across all Curia Massachusetts observations on file
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.22Responsibilities of quality control unit1
The complete Curia Massachusetts file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Burlington, Massachusetts
One Form 483 · 2017 · 2 observations
Latest: Form 483, May 24, 2017 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2017-05-24 | 483 Form 483 | Burlington, Massachusetts | 2 | $99 |
Investigators on these documents
FEI number 3002951540 · most recent document May 24, 2017
About Curia Massachusetts, Inc.
How many FDA Form 483s has Curia Massachusetts, Inc. received?
FDA Intel has 1 Form 483 on file for Curia Massachusetts, Inc.; the most recent is dated May 24, 2017.
When was Curia Massachusetts, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Curia Massachusetts, Inc. is a Form 483 dated May 24, 2017, for the site in Burlington, Massachusetts.
What did FDA cite at Curia Massachusetts, Inc.?
The regulations cited most in the observations on file for Curia Massachusetts, Inc. are 21 CFR 211.113 (Control of microbiological contamination), 1 time; 21 CFR 211.22 (Responsibilities of quality control unit), 1 time.