# FDA Inspection 1048180 - Mortara Sleske - March 08, 2018

Source: https://www.keypedia.com/records/fda_inspections/mortara-sleske/84793619-9b9a-4701-8f34-1eabfabe47f2
Source feed: FDA_Inspections

> FDA Inspection 1048180 for Mortara Sleske on March 08, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1048180
- Company Name: Mortara Sleske
- Inspection Date: 2018-03-08
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/mortara-sleske/a98a8aae-4279-4d48-8b8d-ce8dc1b2056b

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