# Flotec, Inc. – FDA Inspection, May 9, 2013

Source: https://www.keypedia.com/records/fda_inspections/flotec-inc/ca657503-7f40-45fb-9465-c02a90522ce8
Source feed: FDA_Inspections

> FDA inspection 830970 of Flotec, Inc., May 09, 2013. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 3 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 830970
- Company Name: Flotec, Inc.
- Inspection Date: 2013-05-09
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 1132345 - 2019-08-08](https://www.keypedia.com/records/fda_inspections/flotec-inc/339a5daf-60be-4a73-8532-60a9af00b2b4)
- [FDA Inspection 986224 - 2016-09-01](https://www.keypedia.com/records/fda_inspections/flotec-inc/c2a15cfa-6a3a-471c-8ab8-2cc24d4e36d9)
- FDA Inspection 745695 - 2011-09-21

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