# Flexbar Machine Corp – FDA Inspection, Oct 30, 2009

Source: https://www.keypedia.com/records/fda_inspections/flexbar-machine-corp/a287a1cc-38a5-4aa2-a538-55cd8146e835
Source feed: FDA_Inspections

> FDA inspection 625749 of Flexbar Machine Corp, October 30, 2009. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820. 4 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 625749
- Company Name: Flexbar Machine Corp
- Inspection Date: 2009-10-30
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 1266364 - 2025-04-04](https://www.keypedia.com/records/fda_inspections/flexbar-machine-corp/59a67278-7bca-415a-bcf0-85ad1567fb0a)
- [FDA Inspection 1047534 - 2018-04-04](https://www.keypedia.com/records/fda_inspections/flexbar-machine-corp/72c4b31e-b686-46f7-874f-de929e12a4ea)
- FDA Inspection 888627 - 2014-07-22
- FDA Inspection 779265 - 2012-05-01

Company: https://www.keypedia.com/companies/flexbar-machine-corp/9998315c-237d-4866-98c5-8958437449d3

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