# FDA Inspection 1268308 - BIOTECH EUROPE MEDITECH Inc. Ltd - March 26, 2025

Source: https://www.keypedia.com/records/fda_inspections/biotech-europe-meditech-inc-ltd/2e7f171e-bae6-4c34-be13-6502952490a1
Source feed: FDA_Inspections

> FDA Inspection 1268308 for BIOTECH EUROPE MEDITECH Inc. Ltd on March 26, 2025. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1268308
- Company Name: BIOTECH EUROPE MEDITECH Inc. Ltd
- Inspection Date: 2025-03-26
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1268308 - 2025-03-26](https://www.keypedia.com/records/fda_inspections/biotech-europe-meditech-inc-ltd/120801b5-1a65-4e0c-ade2-a980a371bb51)
- [FDA Inspection 1167365 - 2022-04-14](https://www.keypedia.com/records/fda_inspections/biotech-europe-meditech-inc-ltd/2ad39b90-5b24-40da-bfac-f51e0e6a9046)

Company: https://www.keypedia.com/companies/biotech-europe-meditech-inc-ltd/67ada13e-be93-4ee6-b25f-0f0d650bdbca

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7