Thoracent, LLC
FDA inspection history in Huntington, New York, 2025
- 1
- Form 483
Every document, by year
- Form 483
2025: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2025One Form 483, at Huntington, New York.
Cited most
Across all Thoracent observations on file
- 21 CFR 803.17What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?1
- 21 CFR 820.100(a)Corrective and preventive action1
- 21 CFR 820.198(a)Complaint files1
The complete Thoracent file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Huntington, New York
One Form 483 · 2025 · 3 observations
Latest: Form 483, Dec 11, 2025 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-12-11 | 483 Form 483 | Huntington, New York | 3 | $99 |
Investigators on these documents
FEI number 3013337852 · most recent document Dec 11, 2025
About Thoracent, LLC
How many FDA Form 483s has Thoracent, LLC received?
FDA Intel has 1 Form 483 on file for Thoracent, LLC; the most recent is dated Dec 11, 2025.
When was Thoracent, LLC last inspected by FDA?
The most recent FDA inspection document on file for Thoracent, LLC is a Form 483 dated Dec 11, 2025, for the site in Huntington, New York.
What did FDA cite at Thoracent, LLC?
The regulations cited most in the observations on file for Thoracent, LLC are 21 CFR 803.17 (What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?), 1 time; 21 CFR 820.100(a) (Corrective and preventive action), 1 time; 21 CFR 820.198(a) (Complaint files), 1 time.