# Robert Busse & Co., Inc. – FDA Inspection, Oct 10, 2012

Source: https://www.keypedia.com/records/fda_inspections/robert-busse-co-inc/9fe737f2-3738-40ad-8940-7b3279fca3c1
Source feed: FDA_Inspections

> FDA inspection 802601 of Robert Busse & Co., Inc., October 10, 2012. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR parts 803 and 820. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 802601
- Company Name: Robert Busse & Co., Inc.
- Inspection Date: 2012-10-10
- 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: 4

## Related Documents

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- [FDA Inspection 993771 - 2016-10-19](https://www.keypedia.com/records/fda_inspections/robert-busse-co-inc/bfe247ab-e681-4a46-9688-c7f46d170e10)
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Company: https://www.keypedia.com/companies/robert-busse-co-inc/465529b3-d629-44df-860f-10ecdfd3da94

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