# Sienco, Inc – FDA Inspection, Aug 8, 2019

Source: https://www.keypedia.com/records/fda_inspections/sienco-inc/a211b18e-dd8f-4a9f-9a6e-ca26fd3a7bb2
Source feed: FDA_Inspections

> FDA inspection 1100243 of Sienco, Inc, August 08, 2019. Classification: No Action Indicated (NAI). 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1100243
- Company Name: Sienco, Inc
- Inspection Date: 2019-08-08
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- 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 815517 - 2013-01-17
- FDA Inspection 589027 - 2009-06-02

## Related Officers

- [Company Rep](https://www.keypedia.com/people/christine-i-shaw/480cb61e-f173-432d-b84a-c8b492192302)

Company: https://www.keypedia.com/companies/sienco-inc/2737c621-5385-49be-9dd8-bf38017bf6ba

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