# FDA Inspection 1207926 - Lorem Cytori USA - May 19, 2023

Source: https://www.keypedia.com/records/fda_inspections/lorem-cytori-usa/afafa5e8-236b-4729-8292-d86cbe60f838
Source feed: FDA_Inspections

> FDA Inspection 1207926 for Lorem Cytori USA on May 19, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1207926
- Company Name: Lorem Cytori USA
- Inspection Date: 2023-05-19
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1207926 - 2023-05-19](https://www.keypedia.com/records/fda_inspections/lorem-cytori-usa/d852f5e5-f1bc-4326-8f42-4744ff277685)

Company: https://www.keypedia.com/companies/lorem-cytori-usa/d3e192f8-c61f-4190-94c9-e26919e60e82

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