# FDA Inspection 1084312 - ARCH-Quakertown - March 28, 2019

Source: https://www.keypedia.com/records/fda_inspections/arch-quakertown/5e755fa0-5e74-4c92-bab5-b5f0cdd3807a
Source feed: FDA_Inspections

> FDA Inspection 1084312 for ARCH-Quakertown on March 28, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1084312
- Company Name: ARCH-Quakertown
- Inspection Date: 2019-03-28
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1195297 - 2023-01-13](https://www.keypedia.com/records/fda_inspections/arch-quakertown/7a0de4fe-35d1-4de2-978b-0b670e70d69e)

Company: https://www.keypedia.com/companies/arch-quakertown/fce649b2-8d20-412b-a714-617735657c4e

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