# FDA Inspection 911232 - LISI MEDICAL Remmele, Inc - January 14, 2015

Source: https://www.keypedia.com/records/fda_inspections/lisi-medical-remmele-inc/0cc4cdde-70d3-492b-b9a5-48a24b6d6ac4
Source feed: FDA_Inspections

> FDA Inspection 911232 for LISI MEDICAL Remmele, Inc on January 14, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 911232
- Company Name: LISI MEDICAL Remmele, Inc
- Inspection Date: 2015-01-14
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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