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WAVi Co.

FDA Warning Letter · 2023-10-31 · Division of Medical Device and Radiological Health Operations West

Letter

Company
WAVi Co.
Posted Date
2023-10-31
Letter Issue Date
2023-10-20
Issuing Office
Division of Medical Device and Radiological Health Operations West

Subject

Investigational Device Exemptions (IDE)/Premarket Approval Application (PMA) Adulterated Device

Source

Authoritative
FDA Warning Letters
Machine
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