# FDA Inspection 1259508 - Meko - January 30, 2025

Source: https://www.keypedia.com/records/fda_inspections/meko/555646de-8b89-4f35-9b32-d8d54ac3cee3
Source feed: FDA_Inspections

> FDA inspection 1259508 of Meko, January 30, 2025. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1259508
- Company Name: Meko
- Inspection Date: 2025-01-30
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Product Evaluation: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations
- Citation Count: 1

## Related Documents

- 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 996283 - 2017-01-06
- [FDA Inspection 961490 - 2016-02-11](https://www.keypedia.com/records/fda_inspections/meko/7efa2751-6319-4706-a8b0-b104d1a892b4)

## Related Officers

- [Melanie W. Pishnery](https://www.keypedia.com/people/melanie-w-pishnery/ff4846b0-ffe1-4df0-9116-4bb238866b3a)

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

Office: https://www.keypedia.com/offices/office-of-inspections-and-investigations/7dd0b904-a3df-46bc-a7b2-70ddb6f809c8