# CMR Naviscan Corporation – FDA Inspection, Sep 17, 2015

Source: https://www.keypedia.com/records/fda_inspections/cmr-naviscan-corporation/931f9ec8-cc64-4c60-9de9-d0b5ead4b19d
Source feed: FDA_Inspections

> FDA inspection 944056 of CMR Naviscan Corporation, September 17, 2015. Classification: Voluntary Action Indicated (VAI). 4 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 944056
- Company Name: CMR Naviscan Corporation
- Inspection Date: 2015-09-17
- 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: 0

## Related Documents

- [FDA Inspection 1244076 - 2024-07-18](https://www.keypedia.com/records/fda_inspections/cmr-naviscan-corporation/88ba73c5-561a-4e3f-b20e-98aca71e0b6a)
- [FDA Inspection 842544 - 2013-07-31](https://www.keypedia.com/records/fda_inspections/cmr-naviscan-corporation/f318b81d-aceb-4d46-b465-3a51ca20be6e)
- [FDA Inspection 607627 - 2009-08-27](https://www.keypedia.com/records/fda_inspections/cmr-naviscan-corporation/9eb881e0-86c1-4fc9-939f-85b1124bae96)
- FDA Inspection 609252 - 2009-02-11

Company: https://www.keypedia.com/companies/cmr-naviscan-corporation/5d128725-84fb-42f4-83a3-fd5a00385330

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