# CMR Naviscan Corporation – FDA Inspection, Jul 31, 2013

Source: https://www.keypedia.com/records/fda_inspections/cmr-naviscan-corporation/f318b81d-aceb-4d46-b465-3a51ca20be6e
Source feed: FDA_Inspections

> FDA inspection 842544 of CMR Naviscan Corporation, July 31, 2013. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 842544
- Company Name: CMR Naviscan Corporation
- Inspection Date: 2013-07-31
- 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: 3

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- [FDA Inspection 944056 - 2015-09-17](https://www.keypedia.com/records/fda_inspections/cmr-naviscan-corporation/931f9ec8-cc64-4c60-9de9-d0b5ead4b19d)
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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
