# EMSI – FDA Inspection, Jun 15, 2018

Source: https://www.keypedia.com/records/fda_inspections/emsi/7f2d2059-b439-4d14-a137-4ceea9239184
Source feed: FDA_Inspections

> FDA inspection 1056142 of EMSI, June 15, 2018. Classification: No Action Indicated (NAI). 4 citations under 21 CFR part 820. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1056142
- Company Name: EMSI
- Inspection Date: 2018-06-15
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- FDA Inspection 1192319 - 2022-12-08
- [FDA Inspection 893952 - 2014-09-08](https://www.keypedia.com/records/fda_inspections/emsi/b091b147-caff-43bf-9adb-f9ca9a3d3a36)
- 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)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/stanley-b-eugene/4708f43e-0592-4c24-b276-d9f9092788a3)

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