# Frontage Laboratories, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/frontage-laboratories-inc/1705f97d-14a3-4e46-b8a5-220bf2c4799f

> Inspection records and compliance data for Frontage Laboratories, Inc. in Exton, Pennsylvania. Access full analysis and detailed observations.

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## Details

- Name: Frontage Laboratories, Inc.
- FEI Number: 3006799640
- City: Exton
- State: Pennsylvania
- Country Name: United States
- Address Line 1: 700 Pennsylvania Dr
- Zip Code: 19341
- Business Operations: API/FDF ANALYTICAL TESTING

## Related Documents

- [483 - Frontage Laboratories, Inc. - 2026-03-17](https://www.keypedia.com/records/483/frontage-laboratories-inc/efb690f2-9642-44d1-ab0c-5cb8b4cbf547) — source: FDA, date: March 17, 2026
- [FDA Inspection 1281730 - Frontage Laboratories, Inc. - 2025-09-05](https://www.keypedia.com/records/fda_inspections/frontage-laboratories-inc/126db8ad-37a8-42ac-83f5-8e71816154e3) — source: FDA, date: September 5, 2025
- [FDA Inspection 1281730 - Frontage Laboratories, Inc. - 2025-09-05](https://www.keypedia.com/records/fda_inspections/frontage-laboratories-inc/fc8c3d7a-497a-42fa-bee1-442a4076dceb) — classification: No Action Indicated (NAI), source: FDA, date: September 5, 2025
- [483 - Frontage Laboratories, Inc. - 2025-01-10](https://www.keypedia.com/records/483/frontage-laboratories-inc/7fe8a16f-04ae-48ab-a747-3c457bb67fbe) — source: FDA, date: January 10, 2025
- [FDA Inspection 1258228 - Frontage Laboratories, Inc. - 2025-01-10](https://www.keypedia.com/records/fda_inspections/frontage-laboratories-inc/cc35a25e-629e-472d-88b3-cd5216f1f5d1) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 10, 2025
- [FDA Inspection 1258228 - Frontage Laboratories, Inc. - 2025-01-10](https://www.keypedia.com/records/fda_inspections/frontage-laboratories-inc/43866eaf-065b-41b3-81f0-a9e0e3cdfd46) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 10, 2025
- [FDA Inspection 1203309 - Frontage Laboratories, Inc. - 2023-03-31](https://www.keypedia.com/records/fda_inspections/frontage-laboratories-inc/fbd38bf6-e6d7-4ee4-88f5-205e3f8ee054) — classification: No Action Indicated (NAI), source: FDA, date: March 31, 2023
- [483 - Frontage Laboratories, Inc. - 2022-02-18](https://www.keypedia.com/records/483/frontage-laboratories-inc/ff3de5d6-5f98-4168-9b2c-78ac252be164) — source: FDA, date: February 18, 2022
- [EIR - Frontage Laboratories, Inc. - 2022-02-18](https://www.keypedia.com/records/eir/frontage-laboratories-inc/0f20ec9c-5480-467a-b7be-44f4526df94a) — source: FDA, date: February 18, 2022
- [483 - Frontage Laboratories, Inc. - 2021-10-15](https://www.keypedia.com/records/483/frontage-laboratories-inc/0a346dea-dc90-49c2-8c61-75b6ce89ff39) — source: FDA, date: October 15, 2021
- [FDA Inspection 1155307 - Frontage Laboratories, Inc. - 2021-10-15](https://www.keypedia.com/records/fda_inspections/frontage-laboratories-inc/3e753807-5cd1-4232-afce-23e73e74d80c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 15, 2021
- [FDA Inspection 1112214 - Frontage Laboratories, Inc. - 2019-11-01](https://www.keypedia.com/records/fda_inspections/frontage-laboratories-inc/c5aa7f2c-9e34-4c1f-ad4e-f14583800962) — classification: No Action Indicated (NAI), source: FDA, date: November 1, 2019
- [FDA Inspection 1051857 - Frontage Laboratories, Inc. - 2018-04-20](https://www.keypedia.com/records/fda_inspections/frontage-laboratories-inc/76d9cc1a-b11b-48f4-969c-3f62cfc97b62) — classification: No Action Indicated (NAI), source: FDA, date: April 20, 2018
- [FDA Inspection 965450 - Frontage Laboratories, Inc. - 2016-03-18](https://www.keypedia.com/records/fda_inspections/frontage-laboratories-inc/bcde39f0-838c-4f84-9481-83552229b1df) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 18, 2016
- [FDA Inspection 965423 - Frontage Laboratories, Inc. - 2016-03-17](https://www.keypedia.com/records/fda_inspections/frontage-laboratories-inc/f4ddc829-58c4-45e2-b461-e0052034b866) — classification: No Action Indicated (NAI), source: FDA, date: March 17, 2016

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