FDA Inspection
MekoFDA Inspection 961490 - Meko - February 11, 2016
Record Details
This FDA Inspection record concerns Meko, with an inspection on February 11, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Meko
- Inspection Date
- February 11, 2016
- Product Type
- Devices
View Company Profile
ID · 7efa2751-6319-4706-a8b0-b104d1a892b4
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 961490
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Meko
4| Date | Classification | Office | Project area |
|---|---|---|---|
| January 30, 2025 | VAI | Office of Inspections and Investigations | Product Evaluation: Medical Devices |
| November 14, 2024 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
| February 21, 2019 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| January 6, 2017 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Meko
- FDA Inspection 1259508 - 2025-01-30
- FDA Inspection 1256728 - 2024-11-14
- FDA Inspection 1080539 - 2019-02-21
- FDA Inspection 996283 - 2017-01-06
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