# US Endoscopy Group Inc – FDA Inspection, Dec 7, 2016

Source: https://www.keypedia.com/records/fda_inspections/us-endoscopy-group-inc/9605cbe1-1030-49c0-b2c9-2a54c597c954
Source feed: FDA_Inspections

> FDA inspection 994835 of US Endoscopy Group Inc, December 07, 2016. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 994835
- Company Name: US Endoscopy Group Inc
- Inspection Date: 2016-12-07
- 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: 6

## Related Documents

- FDA Inspection 799141 - 2012-09-14
- [FDA Inspection 736932 - 2011-07-21](https://www.keypedia.com/records/fda_inspections/us-endoscopy-group-inc/6801b95a-d1e4-4917-88b3-eba2913fc323)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/laureen-m-geniusz/759a858e-e3f3-4c48-8194-9804c7ab2a7b)

Company: https://www.keypedia.com/companies/us-endoscopy-group-inc/902fcc83-5aed-4aa6-915f-0f9bf25443fe

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