# EMSI – FDA Inspection, Sep 8, 2014

Source: https://www.keypedia.com/records/fda_inspections/emsi/b091b147-caff-43bf-9adb-f9ca9a3d3a36
Source feed: FDA_Inspections

> FDA inspection 893952 of EMSI, September 08, 2014. 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: 893952
- Company Name: EMSI
- Inspection Date: 2014-09-08
- 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

## Related Documents

- FDA Inspection 1192319 - 2022-12-08
- [FDA Inspection 1056142 - 2018-06-15](https://www.keypedia.com/records/fda_inspections/emsi/7f2d2059-b439-4d14-a137-4ceea9239184)
- FDA Inspection 774197 - 2012-03-27
- [FDA Inspection 649429 - 2010-02-24](https://www.keypedia.com/records/fda_inspections/emsi/bfaa6c71-9b32-407c-90ea-2c9aabc858e6)

Company: https://www.keypedia.com/companies/emsi/e0ee00bc-1ff0-4c20-997f-2001d9280480

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