MAVIDON MEDICAL PRODUCTS
FDA inspection history in Flat Rock, North Carolina, 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 Flat Rock, North Carolina.
Cited most
Across all MAVIDON MEDICAL PRODUCTS observations on file
- 21 CFR 820.70(a)Production and process controls3
- 21 CFR 820.50Purchasing controls2
- 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 MAVIDON MEDICAL PRODUCTS file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Flat Rock, North Carolina
One Form 483 · 2025 · 13 observations
Latest: Form 483, Aug 5, 2025 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-08-05 | 483 Form 483 | Flat Rock, North Carolina | 13 | $99 |
Investigators on these documents
FEI number 3017189082 · most recent document Aug 5, 2025
About MAVIDON MEDICAL PRODUCTS
How many FDA Form 483s has MAVIDON MEDICAL PRODUCTS received?
FDA Intel has 1 Form 483 on file for MAVIDON MEDICAL PRODUCTS; the most recent is dated Aug 5, 2025.
When was MAVIDON MEDICAL PRODUCTS last inspected by FDA?
The most recent FDA inspection document on file for MAVIDON MEDICAL PRODUCTS is a Form 483 dated Aug 5, 2025, for the site in Flat Rock, North Carolina.
What did FDA cite at MAVIDON MEDICAL PRODUCTS?
The regulations cited most in the observations on file for MAVIDON MEDICAL PRODUCTS are 21 CFR 820.70(a) (Production and process controls), 3 times; 21 CFR 820.50 (Purchasing controls), 2 times; 21 CFR 803.17 (What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?), 1 time.