# Pacon Manufacturing Corporation – FDA Inspection, Jun 20, 2017

Source: https://www.keypedia.com/records/fda_inspections/pacon-manufacturing-corporation/f6efe85d-32e5-45d4-8939-3483aa11f0cf
Source feed: FDA_Inspections

> FDA inspection 1014922 of Pacon Manufacturing Corporation, June 20, 2017. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1014922
- Company Name: Pacon Manufacturing Corporation
- Inspection Date: 2017-06-20
- 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: 3

## Related Documents

- [FDA Inspection 1120832 - 2020-03-13](https://www.keypedia.com/records/fda_inspections/pacon-manufacturing-corporation/83c0e60a-568c-4ac4-9b58-c44f2d65ffe1)
- [FDA Inspection 974407 - 2016-04-20](https://www.keypedia.com/records/fda_inspections/pacon-manufacturing-corporation/7322628c-eccf-41a1-8c13-d160727cd2fe)
- FDA Inspection 804886 - 2012-10-24
- FDA Inspection 637289 - 2010-01-07

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/esteban-beltran/9a9bf6b2-ecdf-494c-82f4-5ef5932d629a)

Company: https://www.keypedia.com/companies/pacon-manufacturing-corporation/76d5b5c3-3c02-4648-834e-6e49307edc0a

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