# Medtronic CryoCath LP - Inspection Records

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

> Inspection records and compliance data for Medtronic CryoCath LP in Montreal, None. Access full analysis and detailed observations.

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## Details

- Name: Medtronic CryoCath LP
- FEI Number: 3002648230
- City: Montreal
- State: None
- Country Name: Canada
- Address Line 1: 9000 Chemin De Service S
- Zip Code: None

## Related Documents

- [483 - Medtronic CryoCath LP - 2024-10-31](https://www.keypedia.com/records/483/medtronic-cryocath-lp/5ab99a11-3857-47eb-9fec-e77ae07e0e59) — source: FDA, date: October 31, 2024
- [FDA Inspection 1253044 - Medtronic CryoCath LP - 2024-10-31](https://www.keypedia.com/records/fda_inspections/medtronic-cryocath-lp/1e1354f4-4e25-4b06-a7fc-d389d961ed85) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 31, 2024
- [FDA Inspection 1253044 - Medtronic CryoCath LP - 2024-10-31](https://www.keypedia.com/records/fda_inspections/medtronic-cryocath-lp/cda6c9c9-d42e-491a-a810-4bfd86739eb9) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 31, 2024
- [FDA Inspection 1253044 - Medtronic CryoCath LP - 2024-10-31](https://www.keypedia.com/records/fda_inspections/medtronic-cryocath-lp/fe726b2b-3a74-4fb9-8b39-eb444aea9976) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 31, 2024
- [FDA Inspection 1253044 - Medtronic CryoCath LP - 2024-10-31](https://www.keypedia.com/records/fda_inspections/medtronic-cryocath-lp/a9bdba1d-ebc0-4936-8e58-3df10ff326f5) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 31, 2024
- [FDA Inspection 992735 - Medtronic CryoCath LP - 2016-10-27](https://www.keypedia.com/records/fda_inspections/medtronic-cryocath-lp/784c201c-b1f4-4843-bfc6-f3a921408d8e) — classification: No Action Indicated (NAI), source: FDA, date: October 27, 2016
- [FDA Inspection 992735 - Medtronic CryoCath LP - 2016-10-27](https://www.keypedia.com/records/fda_inspections/medtronic-cryocath-lp/e79fd9e7-9dde-4f3f-91d3-b3d7fc73d89b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 27, 2016
- [FDA Inspection 844849 - Medtronic CryoCath LP - 2013-08-15](https://www.keypedia.com/records/fda_inspections/medtronic-cryocath-lp/5e4f69f2-c3ac-4f5f-9836-76fa2389c474) — classification: No Action Indicated (NAI), source: FDA, date: August 15, 2013
- [FDA Inspection 761562 - Medtronic CryoCath LP - 2011-12-16](https://www.keypedia.com/records/fda_inspections/medtronic-cryocath-lp/ebd378f0-6117-4b66-ba5a-45a1a1a0f6c8) — classification: No Action Indicated (NAI), source: FDA, date: December 16, 2011
- [FDA Inspection 761562 - Medtronic CryoCath LP - 2011-12-16](https://www.keypedia.com/records/fda_inspections/medtronic-cryocath-lp/c133b14e-fd61-444c-9e12-5371507f9547) — classification: No Action Indicated (NAI), source: FDA, date: December 16, 2011
- [FDA Inspection 633459 - Medtronic CryoCath LP - 2009-12-10](https://www.keypedia.com/records/fda_inspections/medtronic-cryocath-lp/855db589-127d-45e4-8794-4d1a11c9950d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 10, 2009

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