# FDA Inspection 769752 - Vascutek, Ltd. - February 23, 2012

Source: https://www.keypedia.com/records/fda_inspections/vascutek-ltd/a6ffa148-39ee-4ad1-a953-a4de6db1e8d4
Source feed: FDA_Inspections

> FDA Inspection 769752 for Vascutek, Ltd. on February 23, 2012. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 769752
- Company Name: Vascutek, Ltd.
- Inspection Date: 2012-02-23
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1196234 - 2022-11-17](https://www.keypedia.com/records/fda_inspections/vascutek-ltd/17d43460-63b4-4416-ac30-9cf4576a8aeb)
- [FDA Inspection 769752 - 2012-02-23](https://www.keypedia.com/records/fda_inspections/vascutek-ltd/832bb725-0a03-4af6-bc15-175da1f4d82e)
- [FDA Inspection 769752 - 2012-02-23](https://www.keypedia.com/records/fda_inspections/vascutek-ltd/45a4f287-dcef-4846-a98a-fcb6c0eca703)

Company: https://www.keypedia.com/companies/vascutek-ltd/82db5229-3bbf-4dc3-8c78-cd11b05fcb2c

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