# LISI MEDICAL Remmele, Inc – FDA Inspection, May 1, 2025

Source: https://www.keypedia.com/records/fda_inspections/lisi-medical-remmele-inc/9a561997-957d-4c6d-8bcb-c65efa5c17d9
Source feed: FDA_Inspections

> FDA inspection 1268770 of LISI MEDICAL Remmele, Inc, May 01, 2025. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1268770
- Company Name: LISI MEDICAL Remmele, Inc
- Inspection Date: 2025-05-01
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Minneapolis District Office
- Citation Count: 2

## Related Documents

- [FDA Inspection 1174227 - 2022-07-12](https://www.keypedia.com/records/fda_inspections/lisi-medical-remmele-inc/35dd9ded-785c-402f-8e6b-773c6bc32767)
- FDA Inspection 1041617 - 2018-01-26
- FDA Inspection 911232 - 2015-01-14
- FDA Inspection 561508 - 2009-02-04

## Related Officers

- [Company Rep](https://www.keypedia.com/people/tyler-r-courtney/08ea96c4-cd5a-4793-b7e4-fb2b9ee2b9ef)

Company: https://www.keypedia.com/companies/lisi-medical-remmele-inc/5db0d935-dd79-4f93-9b48-cb429353e242

Office: https://www.keypedia.com/offices/minneapolis-district-office/c79fc8dc-f884-48fc-ba80-2947f662511d