# Alken Inc. – FDA Inspection, Sep 12, 2017

Source: https://www.keypedia.com/records/fda_inspections/alken-inc/a64e298e-920f-40d4-8817-1e5719ed458a
Source feed: FDA_Inspections

> FDA inspection 1027428 of Alken Inc., September 12, 2017. Classification: No Action Indicated (NAI). 3 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1027428
- Company Name: Alken Inc.
- Inspection Date: 2017-09-12
- 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 888714 - 2014-07-24](https://www.keypedia.com/records/fda_inspections/alken-inc/c2eb20c1-64dc-4916-8658-6b9f7680a4c2)
- [FDA Inspection 767900 - 2012-02-16](https://www.keypedia.com/records/fda_inspections/alken-inc/a0a6d37d-d2bd-49dc-891a-668b858e1c3e)
- FDA Inspection 583580 - 2009-05-08

## Related Officers

- Issuing Officer

Company: https://www.keypedia.com/companies/alken-inc/14a582c7-caec-44ec-a2ea-8015997b298b

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