# FDA Inspection 1276435 - LEESAR, INC - July 18, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/leesar-inc/36075330-7622-4ee4-afa7-1cf6e380980b
Source feed: FDA_Inspections

> FDA Inspection 1276435 for LEESAR, INC on July 18, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1276435
- Company Name: LEESAR, INC
- Inspection Date: 2025-07-18
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1276435 - 2025-07-18](https://www.globalkeysolutions.net/records/fda_inspections/leesar-inc/e2518a78-6f9f-4717-bb49-3bbfe1b7d059)
- [FDA Inspection 1276435 - 2025-07-18](https://www.globalkeysolutions.net/records/fda_inspections/leesar-inc/2fb09b50-c6e6-4036-941e-0f75b97575d9)
- [FDA Inspection 1276435 - 2025-07-18](https://www.globalkeysolutions.net/records/fda_inspections/leesar-inc/623b0f78-68fc-4a0d-8ccc-495648d7f252)
- [FDA Inspection 1269588 - 2025-05-09](https://www.globalkeysolutions.net/records/fda_inspections/leesar-inc/5b5e6da8-89f6-4626-8c6e-8ccebe6bbb3d)
- [FDA Inspection 1155647 - 2021-10-29](https://www.globalkeysolutions.net/records/fda_inspections/leesar-inc/32d81905-7783-4221-af38-992e00ec4a4b)

Company: https://www.globalkeysolutions.net/companies/leesar-inc/275b969d-7cd2-4c17-af66-d7ed6ff4dec1

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