# LEESAR, INC – FDA 483, Jul 18, 2025

Source: https://www.keypedia.com/records/483/leesar-inc/c12ff399-e032-40df-9af7-7b45fe5c016f

> FDA 483 for LEESAR, INC on July 18, 2025. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: LEESAR, INC
- Inspection Date: 2025-07-18
- Product Type: device
- Office Name: Florida District Office
- Summary: An FDA inspection of LEESAR, INC in Fort Myers, FL, a repackager/relabeler of Class II medical device EMS kits, revealed two significant observations. The firm failed to establish adequate procedures for management reviews of its quality system pertaining to these kits. Additionally, procedures for quality audits were not adequately established to cover the assembly and distribution of the medical devices.

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- [UNTITLED_LETTER - 2025-04-29](https://www.keypedia.com/records/untitled_letter/leesar-inc/44b860c3-98cb-44d4-82a5-a3df576d2475) — date: April 29, 2025
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Company: https://www.keypedia.com/companies/leesar-inc/275b969d-7cd2-4c17-af66-d7ed6ff4dec1

Office: https://www.keypedia.com/offices/florida-district-office/95b2a118-0b78-46e0-a54c-982bd7ce51c9