# BIOTECH EUROPE MEDITECH Inc. Ltd – FDA Inspection, Mar 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 of BIOTECH EUROPE MEDITECH Inc. Ltd, March 26, 2025. Classification: No Action Indicated (NAI). 1 other FDA inspection on record for this company.

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## 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)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1167365 - 2022-04-14

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/william-r-chang/67893bac-29e2-45b4-ba2c-1ef548781b9c)

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