# FDA Inspection 1201252 - Medisurge, LLC. - March 17, 2023

Source: https://www.keypedia.com/records/fda_inspections/medisurge-llc/12f2eac1-e1a6-4862-84d1-adf5e0d8aa40
Source feed: FDA_Inspections

> FDA Inspection 1201252 for Medisurge, LLC. on March 17, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1201252
- Company Name: Medisurge, LLC.
- Inspection Date: 2023-03-17
- 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 1201252 - 2023-03-17](https://www.keypedia.com/records/fda_inspections/medisurge-llc/e2bcd33e-4781-4a17-a6e2-868f8fdbe88c)
- [FDA Inspection 1062932 - 2018-08-22](https://www.keypedia.com/records/fda_inspections/medisurge-llc/5dae2158-2724-471c-a049-17c40133cabe)
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- [FDA Inspection 909507 - 2015-01-15](https://www.keypedia.com/records/fda_inspections/medisurge-llc/06f9396a-569e-4c04-acb0-75f54b5044fe)

Company: https://www.keypedia.com/companies/medisurge-llc/50d1d25c-fa6d-4e14-80ff-d59386a00731

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