# ARP Manufacturing, LLC – FDA Inspection, Aug 29, 2019

Source: https://www.keypedia.com/records/fda_inspections/arp-manufacturing-llc/8a39c2aa-8555-4264-bf13-fb91e4bf2c5b
Source feed: FDA_Inspections

> FDA inspection 1101458 of ARP Manufacturing, LLC, August 29, 2019. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1101458
- Company Name: ARP Manufacturing, LLC
- Inspection Date: 2019-08-29
- 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: 2

## Related Documents

- FDA Inspection 951685 - 2015-10-16
- [FDA Inspection 755862 - 2011-11-28](https://www.keypedia.com/records/fda_inspections/arp-manufacturing-llc/7abe302c-85b7-48f5-81fa-f7a0ba9cadb0)
- [FDA Inspection 559939 - 2009-01-28](https://www.keypedia.com/records/fda_inspections/arp-manufacturing-llc/514c684d-86a0-4b42-bd50-fa15ac658fec)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/matthew-m-vernon/f77e8c18-8614-49e3-9b19-3327b7fe7648)

Company: https://www.keypedia.com/companies/arp-manufacturing-llc/3f0f5ccb-e7c3-45c2-b5c4-c345fdf79072

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