# CorePharma, LLC - Inspection Records

Source: https://www.keypedia.com/companies/corepharma-llc/037e485c-5d38-40e3-80fe-b00a72cda489

> Inspection records and compliance data for CorePharma, LLC in Middlesex, New Jersey. Access full analysis and detailed observations.

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## Details

- Name: CorePharma, LLC
- FEI Number: 3002535019
- City: Middlesex
- State: New Jersey
- Country Name: United States
- Address Line 1: 215 Wood Ave
- Zip Code: 08846
- Business Operations: API/FDF ANALYTICAL TESTING, FDF MANUFACTURE, PACK

## Related Documents

- [FDA Inspection 1280399 - CorePharma, LLC - 2025-08-28](https://www.keypedia.com/records/fda_inspections/corepharma-llc/2f434b26-30c9-4615-b3f5-50a99beeb527) — source: FDA, date: August 28, 2025
- [FDA Inspection 1280399 - CorePharma, LLC - 2025-08-28](https://www.keypedia.com/records/fda_inspections/corepharma-llc/a79456c1-10bd-4a42-b391-e30e7bd8084c) — classification: No Action Indicated (NAI), source: FDA, date: August 28, 2025
- [FDA Inspection 1240419 - CorePharma, LLC - 2024-09-12](https://www.keypedia.com/records/fda_inspections/corepharma-llc/ab22000e-f850-4fb0-9e5b-5e46d6e93601) — source: FDA, date: September 12, 2024
- [FDA Inspection 1240419 - CorePharma, LLC - 2024-09-12](https://www.keypedia.com/records/fda_inspections/corepharma-llc/debe7cb9-f65c-449a-8bd8-1fa4d1291653) — classification: No Action Indicated (NAI), source: FDA, date: September 12, 2024
- [EIR - CorePharma, LLC - 2019-12-13](https://www.keypedia.com/records/eir/corepharma-llc/87a03a3a-e46c-42f7-9858-c004cff68a0b) — source: FDA, date: December 13, 2019
- [FDA Inspection 1087306 - CorePharma, LLC - 2019-03-29](https://www.keypedia.com/records/fda_inspections/corepharma-llc/2abb9984-6409-4602-b34f-af9a0f281dc6) — classification: No Action Indicated (NAI), source: FDA, date: March 29, 2019
- [FDA Inspection 1029942 - CorePharma, LLC - 2017-10-13](https://www.keypedia.com/records/fda_inspections/corepharma-llc/ca6fc777-a7fa-4962-9541-b11f5137bbaf) — classification: No Action Indicated (NAI), source: FDA, date: October 13, 2017
- [FDA Inspection 980585 - CorePharma, LLC - 2016-08-11](https://www.keypedia.com/records/fda_inspections/corepharma-llc/bc264b16-58fe-4e09-b6d9-d93389a212da) — classification: No Action Indicated (NAI), source: FDA, date: August 11, 2016
- [FDA Inspection 915404 - CorePharma, LLC - 2015-02-24](https://www.keypedia.com/records/fda_inspections/corepharma-llc/580b7a20-2c95-42fd-bbb8-7d184df0d97e) — classification: No Action Indicated (NAI), source: FDA, date: February 24, 2015
- [FDA Inspection 890789 - CorePharma, LLC - 2014-08-12](https://www.keypedia.com/records/fda_inspections/corepharma-llc/6fdb498d-5529-4b6b-bc13-cda83113e8b9) — classification: No Action Indicated (NAI), source: FDA, date: August 12, 2014
- [FDA Inspection 867056 - CorePharma, LLC - 2014-02-21](https://www.keypedia.com/records/fda_inspections/corepharma-llc/a145955f-6754-4aaa-8d82-fc13c19cb6aa) — classification: No Action Indicated (NAI), source: FDA, date: February 21, 2014

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## Related Officers

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- [company_representative](https://www.keypedia.com/people/vithal-dhaduk/3bbc2792-954c-45bc-b0ac-b9b17cab934d)