# FDA Inspection 633459 - Medtronic CryoCath LP - December 10, 2009

Source: https://www.globalkeysolutions.net/records/fda_inspections/medtronic-cryocath-lp/f6a42874-eb4c-4e81-8229-d047672adf12/
Source feed: FDA_Inspections

> FDA Inspection 633459 for Medtronic CryoCath LP on December 10, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 633459
- Company Name: Medtronic CryoCath LP
- Inspection Date: 2009-12-10
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/medtronic-cryocath-lp/af24154a-74f4-435d-beb2-17ce271d1f9b

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