# FDA Inspection 961490 - Meko - February 11, 2016

Source: https://www.keypedia.com/records/fda_inspections/meko/7efa2751-6319-4706-a8b0-b104d1a892b4
Source feed: FDA_Inspections

> FDA inspection 961490 of Meko, February 11, 2016. Classification: Official Action Indicated (OAI). 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 961490
- Company Name: Meko
- Inspection Date: 2016-02-11
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

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Company: https://www.keypedia.com/companies/meko/ee585fb9-ab78-4b2d-8182-cb6fc56da68e

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