# Pacon Manufacturing Corporation, Navassa, NC – FDA Inspections

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

> Inspection records and compliance data for Pacon Manufacturing Corporation in Navassa, North Carolina. 5 FDA inspections on record, 1 Form 483, last inspected March 13, 2020.

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## Details

- Name: Pacon Manufacturing Corporation
- FEI Number: 3015709932
- Address Line 1: 100 Quality Dr Ne
- City: Navassa
- State: North Carolina
- Zip Code: 28451
- Country Name: United States
- Address: 100 Quality Dr Ne, Navassa, North Carolina 28451, United States
- Country: United States

## Related Documents

- [FDA Inspection 1120832 - Pacon Manufacturing Corporation - 2020-03-13](https://www.keypedia.com/records/fda_inspections/pacon-manufacturing-corporation/83c0e60a-568c-4ac4-9b58-c44f2d65ffe1) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 13, 2020
- [FDA Inspection 1014922 - Pacon Manufacturing Corporation - 2017-06-20](https://www.keypedia.com/records/fda_inspections/pacon-manufacturing-corporation/f6efe85d-32e5-45d4-8939-3483aa11f0cf) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 20, 2017
- FDA Inspection 1014922 - Pacon Manufacturing Corporation - 2017-06-20 — classification: No Action Indicated (NAI), source: FDA, date: June 20, 2017
- [FDA Inspection 974407 - Pacon Manufacturing Corporation - 2016-04-20](https://www.keypedia.com/records/fda_inspections/pacon-manufacturing-corporation/7322628c-eccf-41a1-8c13-d160727cd2fe) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 20, 2016
- FDA Inspection 804886 - Pacon Manufacturing Corporation - 2012-10-24 — classification: No Action Indicated (NAI), source: FDA, date: October 24, 2012
- FDA Inspection 804886 - Pacon Manufacturing Corporation - 2012-10-24 — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 24, 2012
- FDA Inspection 637289 - Pacon Manufacturing Corporation - 2010-01-07 — classification: No Action Indicated (NAI), source: FDA, date: January 7, 2010

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