Company
FranceMEDTECH SAS, Montpellier, France – FDA Inspections
Inspection records and compliance data for MEDTECH SAS in Montpellier. 2 FDA inspections on record, 1 Form 483, last inspected July 24, 2025.
Company Profile
This profile covers MEDTECH SAS based in Montpellier, France.
FDA Inspection History
- FDA inspections
- 2
- OAI
- 0
- VAI
- 0
- NAI
- 1
- Unclassified
- 1
- Form 483s
- 1
- Warning letters
- 0
First inspected November 16, 2017. Last inspected July 24, 2025.
Most cited issue areas
- Investigation of device failures1 inspection
- Lack of or inadequate receiving acceptance procedures1 inspection
- Patient Name or Other Identifier1 inspection
FDA inspections (2)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| July 24, 2025 | Not classified | Medical Devices & Rad Health · Compliance: Medical Devices | 1275015 |
| November 16, 2017 | NAI | Medical Devices & Rad Health · Compliance: Devices | 1038442 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
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Company Information
Name
MEDTECH SAS
FEI Number
3009185973
Address
900 Rue Du Mas De Verchant, Montpellier, France
Country
France
ID: 52a4bd61-8d64-4ff4-95b9-a9b8a2f842fb