# FDA Inspection 986224 - Flotec, Inc. - September 01, 2016

Source: https://www.keypedia.com/records/fda_inspections/flotec-inc/c2a15cfa-6a3a-471c-8ab8-2cc24d4e36d9
Source feed: FDA_Inspections

> FDA Inspection 986224 for Flotec, Inc. on September 01, 2016. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 986224
- Company Name: Flotec, Inc.
- Inspection Date: 2016-09-01
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 986224 - 2016-09-01](https://www.keypedia.com/records/fda_inspections/flotec-inc/96a51cef-6302-4577-bf26-0375f6046343)
- [FDA Inspection 830970 - 2013-05-09](https://www.keypedia.com/records/fda_inspections/flotec-inc/ca657503-7f40-45fb-9465-c02a90522ce8)
- [FDA Inspection 745695 - 2011-09-21](https://www.keypedia.com/records/fda_inspections/flotec-inc/ca98388a-93fb-4979-acff-663411b3354f)

Company: https://www.keypedia.com/companies/flotec-inc/fd289515-8fad-4e91-9695-ad4ba724338f

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