# FDA Inspection 953142 - Padtest, LLC - December 21, 2015

Source: https://www.keypedia.com/records/fda_inspections/padtest-llc/bc9b60ea-9c8b-435e-b914-f0a2c8e29a91
Source feed: FDA_Inspections

> FDA Inspection 953142 for Padtest, LLC on December 21, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 953142
- Company Name: Padtest, LLC
- Inspection Date: 2015-12-21
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1170507 - 2022-04-28](https://www.keypedia.com/records/fda_inspections/padtest-llc/d362e416-5e7a-4cbc-ba4a-cac4559e769e)
- [FDA Inspection 1170507 - 2022-04-28](https://www.keypedia.com/records/fda_inspections/padtest-llc/a9bdd127-2da9-4adb-88b9-026f5e8446ff)

Company: https://www.keypedia.com/companies/padtest-llc/42be1131-956d-4ff8-b68b-bd7c3dd24b61

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