# LISI MEDICAL Remmele, Inc – FDA Inspection, Jul 12, 2022

Source: https://www.keypedia.com/records/fda_inspections/lisi-medical-remmele-inc/35dd9ded-785c-402f-8e6b-773c6bc32767
Source feed: FDA_Inspections

> FDA inspection 1174227 of LISI MEDICAL Remmele, Inc, July 12, 2022. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1174227
- Company Name: LISI MEDICAL Remmele, Inc
- Inspection Date: 2022-07-12
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 1268770 - 2025-05-01](https://www.keypedia.com/records/fda_inspections/lisi-medical-remmele-inc/9a561997-957d-4c6d-8bcb-c65efa5c17d9)
- FDA Inspection 1041617 - 2018-01-26
- FDA Inspection 911232 - 2015-01-14
- FDA Inspection 561508 - 2009-02-04

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

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