M.D.L. S.R.L.
1 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (1)
- Inspections (2)
Devices registered here (1)
- Instrument, BiopsyProduct code KNW (opens in a new tab) · Class II · Gastroenterology, Urology · 21 CFR 876.1075
Recalls & enforcement
- Class IITerminated2021-08-05Sterility assurance may be compromised.
FDA inspections (2)
- NAI2024-02-15No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices
- VAI2019-09-19Voluntary Action Indicated · Compliance: Devices · citations posted
Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.
Related
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)
Cite this record
RegWarden. “M.D.L. S.R.L. (FEI 3004749705) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3004749705-m-d-l-s-r-l/
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