# Medtronic CryoCath LP – FDA Inspection, Dec 16, 2011

Source: https://www.keypedia.com/records/fda_inspections/medtronic-cryocath-lp/ebd378f0-6117-4b66-ba5a-45a1a1a0f6c8
Source feed: FDA_Inspections

> FDA inspection 761562 of Medtronic CryoCath LP, December 16, 2011. Classification: No Action Indicated (NAI). 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 761562
- Company Name: Medtronic CryoCath LP
- Inspection Date: 2011-12-16
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1253044 - 2024-10-31](https://www.keypedia.com/records/fda_inspections/medtronic-cryocath-lp/cda6c9c9-d42e-491a-a810-4bfd86739eb9)
- [FDA Inspection 992735 - 2016-10-27](https://www.keypedia.com/records/fda_inspections/medtronic-cryocath-lp/e79fd9e7-9dde-4f3f-91d3-b3d7fc73d89b)
- FDA Inspection 844849 - 2013-08-15
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Company: https://www.keypedia.com/companies/medtronic-cryocath-lp/af24154a-74f4-435d-beb2-17ce271d1f9b

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