RegWardenFDA facility compliance records
Facility

ADRIA SRL.

1 recall(s) on record — most severe on record: Class II.

Activity by year

FDA actions on record by year2021: 1 recalls; 2023: 1 inspections201720182019202012021202212023202420252026
  • Recalls (1)
  • Inspections (1)

Devices registered here (1)

Recalls & enforcement

  • Class IITerminated2021-05-17
    The recalling firm was notified by the contract sterilizer that the process parameters of the sterilization cycles were not followed.

FDA inspections (1)

  • VAI2023-03-16
    Voluntary Action Indicated · Compliance: Devices; Postmarket Assurance: 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. “ADRIA SRL. (FEI 3014200871) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3014200871-adria-srl/

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