# FDA Inspection 976158 - E K Industries Inc - June 02, 2016

Source: https://www.keypedia.com/records/fda_inspections/e-k-industries-inc/f116bd4f-c1e5-4646-8a64-eb13e110f815
Source feed: FDA_Inspections

> FDA Inspection 976158 for E K Industries Inc on June 02, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 976158
- Company Name: E K Industries Inc
- Inspection Date: 2016-06-02
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/e-k-industries-inc/8db7bfaf-4fef-4d70-93de-b9f76d2fe918

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