# FDA Inspection 971033 - Sequel Special Products, LLC - May 18, 2016

Source: https://www.keypedia.com/records/fda_inspections/sequel-special-products-llc/8655d2be-102e-4ca6-9755-4bdeee08ef80
Source feed: FDA_Inspections

> FDA Inspection 971033 for Sequel Special Products, LLC on May 18, 2016. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 971033
- Company Name: Sequel Special Products, LLC
- Inspection Date: 2016-05-18
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1117093 - 2020-01-28](https://www.keypedia.com/records/fda_inspections/sequel-special-products-llc/178e1c8a-cb88-4594-ae72-9826fc89e26a)
- [FDA Inspection 1117093 - 2020-01-28](https://www.keypedia.com/records/fda_inspections/sequel-special-products-llc/f458ba68-609d-4ec7-a43b-d24556c107b4)
- [FDA Inspection 971033 - 2016-05-18](https://www.keypedia.com/records/fda_inspections/sequel-special-products-llc/40d25a70-660e-49e6-b22e-9de82da143a9)

Company: https://www.keypedia.com/companies/sequel-special-products-llc/fb875011-ce73-4b6f-9c4f-954c1806cd80

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