# FDA Inspection 1200171 - Keller Laboratories - March 17, 2023

Source: https://www.keypedia.com/records/fda_inspections/keller-laboratories/412eee6f-cf87-4da3-8a7e-27a4605a7ac8
Source feed: FDA_Inspections

> FDA Inspection 1200171 for Keller Laboratories on March 17, 2023. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1200171
- Company Name: Keller Laboratories
- Inspection Date: 2023-03-17
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1200171 - 2023-03-17](https://www.keypedia.com/records/fda_inspections/keller-laboratories/5352343e-26f5-4323-a2a4-c43d4d4bac3e)
- [FDA Inspection 1051759 - 2018-05-10](https://www.keypedia.com/records/fda_inspections/keller-laboratories/7917b00a-1542-441c-8c7a-52e2bfbe4616)
- [FDA Inspection 1051759 - 2018-05-10](https://www.keypedia.com/records/fda_inspections/keller-laboratories/5433423b-f6ec-4cd9-b659-81c600674989)
- [FDA Inspection 882874 - 2014-06-11](https://www.keypedia.com/records/fda_inspections/keller-laboratories/8531d71a-aac7-490f-8311-63264b421d82)
- [FDA Inspection 882874 - 2014-06-11](https://www.keypedia.com/records/fda_inspections/keller-laboratories/79223d74-ad6c-449b-8d5c-23fe034b5b81)

Company: https://www.keypedia.com/companies/keller-laboratories/7cff8918-be58-467a-904d-3a4095742bc9

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