FDA Inspection
Pacon Manufacturing CorporationPacon Manufacturing Corporation – FDA Inspection, Mar 13, 2020
Record Details
This FDA Inspection record concerns Pacon Manufacturing Corporation, with an inspection on March 13, 2020, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- March 13, 2020
- Product Type
- Devices
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ID · 83c0e60a-568c-4ac4-9b58-c44f2d65ffe1
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1120832
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.70(e)Contamination control, Lack of or inadequate procedures
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Other FDA inspections of Pacon Manufacturing Corporation
4| Date | Classification | Office | Project area |
|---|---|---|---|
| June 20, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 20, 2016 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| October 24, 2012 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| January 7, 2010 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Pacon Manufacturing Corporation
- FDA Inspection 1014922 - 2017-06-20
- FDA Inspection 974407 - 2016-04-20
- FDA Inspection 804886 - 2012-10-24
- FDA Inspection 637289 - 2010-01-07
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