# FDA Inspection 1280952 - CTL BIOTEC - June 19, 2025

Source: https://www.keypedia.com/records/fda_inspections/ctl-biotec/b1af71d2-fe51-4f9d-b9c3-66b8b90e3397
Source feed: FDA_Inspections

> FDA Inspection 1280952 for CTL BIOTEC on June 19, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1280952
- Company Name: CTL BIOTEC
- Inspection Date: 2025-06-19
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1280952 - 2025-06-19](https://www.keypedia.com/records/fda_inspections/ctl-biotec/30a3bd93-4fae-4786-b3f6-e94b98ac2f0b)
- [FDA Inspection 1280952 - 2025-06-19](https://www.keypedia.com/records/fda_inspections/ctl-biotec/5aedfd97-de90-4488-97f3-ede5800881ac)

Company: https://www.keypedia.com/companies/ctl-biotec/0055cb58-77a6-4139-acf9-7022fafa6541

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