FDA Inspection
Mevion Medical Systems, Inc.Mevion Medical Systems, Inc. – FDA Inspection, Aug 24, 2018
Record Details
This FDA Inspection record concerns Mevion Medical Systems, Inc., with an inspection on August 24, 2018, issued by the New England District Office, covering medical devices & rad health.
- Company
- Mevion Medical Systems, Inc.
- Inspection Date
- August 24, 2018
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · 983d318f-66a5-4ce2-90ac-18dd17670f28
Inspection Facts
- Inspection number
- 1132619
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Mevion Medical Systems, Inc.
5| Date | Classification | Office | Project area |
|---|---|---|---|
| October 9, 2024 | Not classified | New England District Office | Compliance: Medical Devices |
| March 5, 2020 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| March 30, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 16, 2015 | VAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
| September 6, 2012 | NAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
Other documents for Mevion Medical Systems, Inc.
- FDA Inspection 1251608 - 2024-10-09
- FDA Inspection 1120302 - 2020-03-05
- FDA Inspection 1005904 - 2017-03-30
- FDA Inspection 918036 - 2015-03-16
- FDA Inspection 797581 - 2012-09-06
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