# Frontida BioPharm Inc, Philadelphia, PA – FDA Inspections

Source: https://www.keypedia.com/companies/frontida-biopharm-inc/dc8190f9-0e13-4160-a611-dcf664f43b09

> Inspection records and compliance data for Frontida BioPharm Inc in Philadelphia, Pennsylvania. 15 FDA inspections on record (1 OAI), 3 Form 483s, last inspected April 02, 2026.

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## Details

- Name: Frontida BioPharm Inc
- FEI Number: 2523348
- Business Operations: API/FDF ANALYTICAL TESTING, FDF MANUFACTURE, PACK
- Address Line 1: 1100 Orthodox St
- City: Philadelphia
- State: Pennsylvania
- Zip Code: 19124
- Country Name: United States
- Address: 1100 Orthodox St, Philadelphia, Pennsylvania 19124, United States
- Country: United States

## Related Documents

- FDA Inspection 1316756 - Frontida BioPharm Inc - 2026-04-02 — source: FDA, date: April 2, 2026
- FDA Inspection 1279864 - Frontida BioPharm Inc - 2025-07-22 — source: FDA, date: July 22, 2025
- FDA Inspection 1280570 - Frontida BioPharm Inc - 2025-07-22 — classification: No Action Indicated (NAI), source: FDA, date: July 22, 2025
- [FDA Inspection 1279864 - Frontida BioPharm Inc - 2025-07-22](https://www.keypedia.com/records/fda_inspections/frontida-biopharm-inc/be6ada2f-716c-4ddd-8b36-f7d3b7cd65b3) — classification: No Action Indicated (NAI), source: FDA, date: July 22, 2025
- [483 - Frontida BioPharm Inc - 2023-12-07](https://www.keypedia.com/records/483/frontida-biopharm-inc/c91263e1-f4e2-4769-aada-9f498f973d1f) — source: FDA, date: December 7, 2023
- [FDA Inspection 1226606 - Frontida BioPharm Inc - 2023-12-07](https://www.keypedia.com/records/fda_inspections/frontida-biopharm-inc/9b8055f0-3548-413c-a40b-5814226a9434) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 7, 2023
- [FDA Inspection 1097023 - Frontida BioPharm Inc - 2019-07-19](https://www.keypedia.com/records/fda_inspections/frontida-biopharm-inc/19fa9164-4fb0-41e4-9013-e9731116e4ad) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 19, 2019
- FDA Inspection 1030391 - Frontida BioPharm Inc - 2017-07-20 — source: FDA, date: July 20, 2017
- [FDA Inspection 1007832 - Frontida BioPharm Inc - 2017-03-31](https://www.keypedia.com/records/fda_inspections/frontida-biopharm-inc/ecd75cf3-3eb9-47eb-a2f2-38adbdb18510) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 31, 2017
- [FDA Inspection 936055 - Frontida BioPharm Inc - 2015-07-17](https://www.keypedia.com/records/fda_inspections/frontida-biopharm-inc/2cf91318-6f6b-4647-a138-7593f304329e) — classification: Official Action Indicated (OAI), source: FDA, date: July 17, 2015
- FDA Inspection 890268 - Frontida BioPharm Inc - 2014-07-25 — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 25, 2014

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