# FDA Inspection 1080539 - Meko - February 21, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/meko/ac123f33-591a-47df-9404-80d43b4eedf2
Source feed: FDA_Inspections

> FDA Inspection 1080539 for Meko on February 21, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1080539
- Company Name: Meko
- Inspection Date: 2019-02-21
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/meko/ee585fb9-ab78-4b2d-8182-cb6fc56da68e

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