# FDA Inspection 1051759 - Keller Laboratories - May 10, 2018

Source: https://www.keypedia.com/records/fda_inspections/keller-laboratories/5433423b-f6ec-4cd9-b659-81c600674989
Source feed: FDA_Inspections

> FDA Inspection 1051759 for Keller Laboratories on May 10, 2018. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1051759
- Company Name: Keller Laboratories
- Inspection Date: 2018-05-10
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1311068 - 2026-04-06](https://www.keypedia.com/records/fda_inspections/keller-laboratories/e55ea529-969e-448e-9085-ad2379862424)
- [FDA Inspection 1311068 - 2026-04-06](https://www.keypedia.com/records/fda_inspections/keller-laboratories/d2de8684-07df-47d4-839d-9cee33b48218)
- [FDA Inspection 1200171 - 2023-03-17](https://www.keypedia.com/records/fda_inspections/keller-laboratories/412eee6f-cf87-4da3-8a7e-27a4605a7ac8)
- [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)

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