RegWardenFDA facility compliance records
Facility

Oxus America, Inc.

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

Activity by year

FDA actions on record by year2013: 1 recalls; 2016: 1 inspections; 2019: 1 inspections1’13’14’151’16’17’181’19’20’21’22’23’24’25’26
  • Recalls (1)
  • Inspections (2)

Devices registered here (1)

Recalls & enforcement

  • Class IITerminated2013-01-14
    Due to past battery inventory storage conditions and deficiencies in the maintenance procedure, it was possible that some batteries were over-discharged to point of damaging the cells.

FDA inspections (2)

  • NAI2019-10-10
    No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
  • VAI2016-01-19
    Voluntary 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. “Oxus America, Inc. (FEI 3008841036) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3008841036-oxus-america-inc/

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