# LISI MEDICAL Remmele, Inc – FDA Inspection, Apr 27, 2023

Source: https://www.keypedia.com/records/fda_inspections/lisi-medical-remmele-inc/8a42ee05-e6b2-4e55-b07e-f62e1b77c7ed
Source feed: FDA_Inspections

> FDA inspection 1203796 of LISI MEDICAL Remmele, Inc, April 27, 2023. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1203796
- Company Name: LISI MEDICAL Remmele, Inc
- Inspection Date: 2023-04-27
- 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 1041633 - 2018-01-18
- FDA Inspection 910759 - 2015-01-14

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/mildred-j-tures/c21df23d-580f-4cdc-94a1-194d981e41be)

Company: https://www.keypedia.com/companies/lisi-medical-remmele-inc/5779aae4-d823-45e4-8c6e-0dbe63df72cb

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