# Medtronic CryoCath LP – FDA Inspection, Oct 27, 2016

Source: https://www.keypedia.com/records/fda_inspections/medtronic-cryocath-lp/e79fd9e7-9dde-4f3f-91d3-b3d7fc73d89b
Source feed: FDA_Inspections

> FDA inspection 992735 of Medtronic CryoCath LP, October 27, 2016. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820. Form 483 issued. 4 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 992735
- Company Name: Medtronic CryoCath LP
- Inspection Date: 2016-10-27
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## 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 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

- [Investigator](https://www.keypedia.com/people/catherine-j-laufmann/920b7656-2847-408d-ba15-3989283d8c94)

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