# Vygon MFG, Inc. – FDA Inspection, May 21, 2018

Source: https://www.keypedia.com/records/fda_inspections/vygon-mfg-inc/588d3aaa-53c1-4b58-82bb-1a9e57e4de14
Source feed: FDA_Inspections

> FDA inspection 1054315 of Vygon MFG, Inc., May 21, 2018. Classification: No Action Indicated (NAI). 1 citation 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: 1054315
- Company Name: Vygon MFG, Inc.
- Inspection Date: 2018-05-21
- 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: 1

## Related Documents

- [FDA Inspection 986397 - 2016-09-23](https://www.keypedia.com/records/fda_inspections/vygon-mfg-inc/b7b1eaac-6bb7-4928-83fb-e8cb72fa3a35)
- FDA Inspection 848668 - 2013-09-05
- FDA Inspection 735332 - 2011-07-28
- FDA Inspection 702972 - 2010-12-17
- [FDA Inspection 577818 - 2009-02-18](https://www.keypedia.com/records/fda_inspections/vygon-mfg-inc/c58f3b8d-a5de-419c-a9fa-e4e511a1b743)

## Related Officers

- Issuing Officer

Company: https://www.keypedia.com/companies/vygon-mfg-inc/609245ef-6ebb-4020-8ef6-43be921cb444

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