# FDA Inspection 1094240 - REBOUND THERAPEUTICS, CORPORATION - May 16, 2019

Source: https://www.keypedia.com/records/fda_inspections/rebound-therapeutics-corporation/652c55c1-d238-4271-aee5-e942ec8c2ba7
Source feed: FDA_Inspections

> FDA Inspection 1094240 for REBOUND THERAPEUTICS, CORPORATION on May 16, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1094240
- Company Name: REBOUND THERAPEUTICS, CORPORATION
- Inspection Date: 2019-05-16
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1094240 - 2019-05-16](https://www.keypedia.com/records/fda_inspections/rebound-therapeutics-corporation/bec1e1cc-a028-4a34-bf99-6dd2272fb0f4)

Company: https://www.keypedia.com/companies/rebound-therapeutics-corporation/eb71e06e-201a-45c8-a704-3db2894800b8

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7