# Sonneborn, LLC - Inspection Records

Source: https://www.keypedia.com/companies/sonneborn-llc/a3b94b8f-4ffb-4c19-9bb5-b8cfc23c7f58

> Inspection records and compliance data for Sonneborn, LLC in Petrolia, PA. Access full analysis and detailed observations.

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## Details

- Name: Sonneborn, LLC
- FEI Number: 2515782
- City: Petrolia
- State: PA
- Country Name: United States
- Address Line 1: 100 Sonneborn Lane
- Zip Code: 16050

## Related Documents

- [483 - Sonneborn, LLC - 2025-08-20](https://www.keypedia.com/records/483/sonneborn-llc/124f0170-85ba-4a97-be56-280484f77bba) — source: FDA, date: August 20, 2025
- [FDA Inspection 1280535 - Sonneborn, LLC - 2025-08-20](https://www.keypedia.com/records/fda_inspections/sonneborn-llc/e275a792-1274-4989-b676-cb00690e1cc9) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 20, 2025
- [EIR - Sonneborn, LLC - 2021-11-01](https://www.keypedia.com/records/eir/sonneborn-llc/fdaa8a6f-e566-46ad-a364-038639ddd23a) — source: FDA, date: November 1, 2021
- [FDA Inspection 1157425 - Sonneborn, LLC - 2021-11-01](https://www.keypedia.com/records/fda_inspections/sonneborn-llc/bb5f91e5-36fd-4b25-b76e-499d945a7818) — classification: No Action Indicated (NAI), source: FDA, date: November 1, 2021
- [EIR - Sonneborn, LLC - 2019-07-10](https://www.keypedia.com/records/eir/sonneborn-llc/23dce118-933d-409b-a08a-ca5035e5a415) — source: FDA, date: July 10, 2019
- [FDA Inspection 1101694 - Sonneborn, LLC - 2019-07-10](https://www.keypedia.com/records/fda_inspections/sonneborn-llc/a005c0ee-6954-4ee7-ad75-c875ce989c03) — classification: No Action Indicated (NAI), source: FDA, date: July 10, 2019
- [EIR - Sonneborn, LLC - 2018-09-12](https://www.keypedia.com/records/eir/sonneborn-llc/47303258-c004-4e85-bf7d-ea5166610e71) — source: FDA, date: September 12, 2018
- [FDA Inspection 1070715 - Sonneborn, LLC - 2018-09-12](https://www.keypedia.com/records/fda_inspections/sonneborn-llc/483497c7-72ab-4126-ae6e-46a3e5313b37) — classification: No Action Indicated (NAI), source: FDA, date: September 12, 2018
- [FDA Inspection 1070715 - Sonneborn, LLC - 2018-09-12](https://www.keypedia.com/records/fda_inspections/sonneborn-llc/90d4f475-202e-4013-8b9e-42f944e46a3c) — classification: No Action Indicated (NAI), source: FDA, date: September 12, 2018
- [EIR - Sonneborn, LLC - 2014-06-30](https://www.keypedia.com/records/eir/sonneborn-llc/9b97b086-bf46-45f1-bb75-00780d9a097e) — source: FDA, date: June 30, 2014
- [FDA Inspection 885420 - Sonneborn, LLC - 2014-06-30](https://www.keypedia.com/records/fda_inspections/sonneborn-llc/bb248f27-e407-4c46-ae57-907a79b35f7c) — classification: No Action Indicated (NAI), source: FDA, date: June 30, 2014
- [FDA Inspection 885420 - Sonneborn, LLC - 2014-06-30](https://www.keypedia.com/records/fda_inspections/sonneborn-llc/2037faa2-d374-4928-8398-9554e065a6e7) — classification: No Action Indicated (NAI), source: FDA, date: June 30, 2014
- [FDA Inspection 672051 - Sonneborn, LLC - 2010-06-24](https://www.keypedia.com/records/fda_inspections/sonneborn-llc/05a949bb-eb13-4043-886b-1e1d5ea7e0ea) — classification: No Action Indicated (NAI), source: FDA, date: June 24, 2010
- [FDA Inspection 592103 - Sonneborn, LLC - 2009-05-28](https://www.keypedia.com/records/fda_inspections/sonneborn-llc/a0674a02-f8db-4dd1-9d37-c0f020f5bd56) — classification: No Action Indicated (NAI), source: FDA, date: May 28, 2009

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