# Robert Busse & Co., Inc. – FDA Inspection, Apr 13, 2018

Source: https://www.keypedia.com/records/fda_inspections/robert-busse-co-inc/ed8ed895-324b-4d60-8803-a05263018c32
Source feed: FDA_Inspections

> FDA inspection 1048678 of Robert Busse & Co., Inc., April 13, 2018. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1048678
- Company Name: Robert Busse & Co., Inc.
- Inspection Date: 2018-04-13
- 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 993771 - 2016-10-19](https://www.keypedia.com/records/fda_inspections/robert-busse-co-inc/bfe247ab-e681-4a46-9688-c7f46d170e10)
- [FDA Inspection 918565 - 2015-02-27](https://www.keypedia.com/records/fda_inspections/robert-busse-co-inc/ca653ff5-fe52-4645-9b97-ceeee8eb985b)
- [FDA Inspection 802601 - 2012-10-10](https://www.keypedia.com/records/fda_inspections/robert-busse-co-inc/9fe737f2-3738-40ad-8940-7b3279fca3c1)
- FDA Inspection 719303 - 2011-04-11
- FDA Inspection 546561 - 2008-11-07

## Related Officers

- [Company Rep](https://www.keypedia.com/people/ronald-ifraimov/b4ce8b79-3fa2-4862-b7a4-68e14e45d87a)

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