# FDA Inspection 697318 - Electrotek Corporation - October 14, 2010

Source: https://www.keypedia.com/records/fda_inspections/electrotek-corporation/0ed67d09-5817-4ab5-8c0c-6aee7fdfed99
Source feed: FDA_Inspections

> FDA Inspection 697318 for Electrotek Corporation on October 14, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 697318
- Company Name: Electrotek Corporation
- Inspection Date: 2010-10-14
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/electrotek-corporation/41ffdce8-141c-4017-bccf-d4f40b5459ef

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