# FDA Inspection 1101458 - ARP Manufacturing, LLC - August 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 for ARP Manufacturing, LLC on August 29, 2019. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

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- [FDA Inspection 951685 - 2015-10-16](https://www.keypedia.com/records/fda_inspections/arp-manufacturing-llc/a02f4269-6474-4b4a-9aa5-a2632bcc8950)
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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