# Meko – FDA Inspection, Jan 6, 2017

Source: https://www.keypedia.com/records/fda_inspections/meko/2d2b0164-faf9-4213-a877-968af2437306
Source feed: FDA_Inspections

> FDA inspection 996283 of Meko, January 06, 2017. Classification: No Action Indicated (NAI). Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 996283
- Company Name: Meko
- Inspection Date: 2017-01-06
- 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 1259508 - 2025-01-30](https://www.keypedia.com/records/fda_inspections/meko/555646de-8b89-4f35-9b32-d8d54ac3cee3)
- FDA Inspection 1256728 - 2024-11-14
- [FDA Inspection 1080539 - 2019-02-21](https://www.keypedia.com/records/fda_inspections/meko/ac123f33-591a-47df-9404-80d43b4eedf2)
- [FDA Inspection 961490 - 2016-02-11](https://www.keypedia.com/records/fda_inspections/meko/7efa2751-6319-4706-a8b0-b104d1a892b4)

## Related Officers

- [Sean T. Creighton](https://www.keypedia.com/people/sean-t-creighton/80ffecab-0a2d-4727-a11f-407b697f4503)

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