# Robert Busse & Co., Inc. – FDA Inspection, Oct 19, 2016

Source: https://www.keypedia.com/records/fda_inspections/robert-busse-co-inc/bfe247ab-e681-4a46-9688-c7f46d170e10
Source feed: FDA_Inspections

> FDA inspection 993771 of Robert Busse & Co., Inc., October 19, 2016. Classification: No Action Indicated (NAI). 6 citations under 21 CFR parts 211 and 820. Form 483 issued. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 993771
- Company Name: Robert Busse & Co., Inc.
- Inspection Date: 2016-10-19
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 6

## Related Documents

- [FDA Inspection 1048678 - 2018-04-13](https://www.keypedia.com/records/fda_inspections/robert-busse-co-inc/ed8ed895-324b-4d60-8803-a05263018c32)
- [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

- [Dipesh K. Shah](https://www.keypedia.com/people/dipesh-k-shah/d4df4040-13d1-477b-8c21-4c8e5b3fc5b9)

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