# FDA Inspection 735640 - OXFORD IMMUNOTEC INC DBA IMUGEN - July 21, 2011

Source: https://www.globalkeysolutions.net/records/fda_inspections/oxford-immunotec-inc-dba-imugen/fca33f35-48b1-426b-814e-8bbf5634ac16/
Source feed: FDA_Inspections

> FDA Inspection 735640 for OXFORD IMMUNOTEC INC DBA IMUGEN on July 21, 2011. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 735640
- Company Name: OXFORD IMMUNOTEC INC DBA IMUGEN
- Inspection Date: 2011-07-21
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 845914 - 2013-08-16](https://www.globalkeysolutions.net/api/records/fda_inspections/oxford-immunotec-inc-dba-imugen/6a98f294-4856-427d-8aac-ed1514be1b7e/)

Company: https://www.globalkeysolutions.net/companies/oxford-immunotec-inc-dba-imugen/6aa4b40f-8fb8-46ce-88f2-129db1c6131f

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