# Medtronic CryoCath LP – FDA Inspection, Oct 31, 2024

Source: https://www.keypedia.com/records/fda_inspections/medtronic-cryocath-lp/cda6c9c9-d42e-491a-a810-4bfd86739eb9
Source feed: FDA_Inspections

> FDA inspection 1253044 of Medtronic CryoCath LP, October 31, 2024. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1253044
- Company Name: Medtronic CryoCath LP
- Inspection Date: 2024-10-31
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations
- Citation Count: 1

## Related Documents

- [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
- [FDA Inspection 761562 - 2011-12-16](https://www.keypedia.com/records/fda_inspections/medtronic-cryocath-lp/ebd378f0-6117-4b66-ba5a-45a1a1a0f6c8)
- FDA Inspection 633459 - 2009-12-10

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/felix-j-marrero/fe3bf64e-987b-40d9-8a17-754d58e13433)

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

Office: https://www.keypedia.com/offices/office-of-inspections-and-investigations/7dd0b904-a3df-46bc-a7b2-70ddb6f809c8