RightEye, LLC
FDA warning letter issued 2022-12-20 · posted 2023-01-31
Letter details
- Company
- RightEye, LLC
- Subject
- Investigational Device Exemptions (IDE)/Premarket Approval Application (PMA) Adulterated Device
- Issuing office
- Division of Medical Device and Radiological Health Operations East
- Letter issue date
- 2022-12-20
- Posted date
- 2023-01-31
- Case number
- 643192
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