# FDA Inspection 1276436 - Leesar Inc - July 18, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/leesar-inc/33d283cb-b330-4336-8dc3-fa43b19c4e9c
Source feed: FDA_Inspections

> FDA Inspection 1276436 for Leesar Inc on July 18, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1276436
- Company Name: Leesar Inc
- Inspection Date: 2025-07-18
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1276436 - 2025-07-18](https://www.globalkeysolutions.net/records/fda_inspections/leesar-inc/5002f213-fa78-46f3-aee1-c9a8f6892fce)
- [FDA Inspection 1276436 - 2025-07-18](https://www.globalkeysolutions.net/records/fda_inspections/leesar-inc/0d5d587f-616d-4293-8403-afdbc71f5986)
- [FDA Inspection 1276436 - 2025-07-18](https://www.globalkeysolutions.net/records/fda_inspections/leesar-inc/a7cea93b-f937-4095-a967-6c2bc91f8336)

Company: https://www.globalkeysolutions.net/companies/leesar-inc/91c4b528-bf5a-4e1e-a96d-5244bfcf3781

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