FDA Inspection
MekoMeko – FDA Inspection, Jan 6, 2017
Record Details
This FDA Inspection record concerns Meko, with an inspection on January 6, 2017, issued by the Center for Devices and Radiological Health, covering devices.
View Company Profile
ID · 2d2b0164-faf9-4213-a877-968af2437306
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 996283
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
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 |
| February 11, 2016 | OAI | 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 961490 - 2016-02-11
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.