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DRG Instruments GmbH

FDA Warning Letter · 2025-05-27 · Center for Devices and Radiological Health

Letter

Company
DRG Instruments GmbH
Posted Date
2025-05-27
Letter Issue Date
2025-03-31
Issuing Office
Center for Devices and Radiological Health

Subject

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

Source

Authoritative
FDA Warning Letters
Machine
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