# Altora Pharma Solutions LLC - Inspection Records

Source: https://www.globalkeysolutions.net/companies/altora-pharma-solutions-llc/9a13bcb2-ffcb-4600-a334-b6f200ee9f4f

> Inspection records and compliance data for Altora Pharma Solutions LLC in Decatur, Georgia. Access full analysis and detailed observations.

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## Details

- Name: Altora Pharma Solutions LLC
- FEI Number: 3010659365
- City: Decatur
- State: Georgia
- Country Name: United States
- Address Line 1: 2443 Park Central Blvd
- Zip Code: 30035

## Related Documents

- [FDA Inspection 1300974 - Altora Pharma Solutions LLC - 2026-01-15](https://www.globalkeysolutions.net/records/fda_inspections/altora-pharma-solutions-llc/a95d3059-0da2-43b4-bb1e-e8b837d5d88a) — source: FDA, date: January 15, 2026
- [FDA Inspection 1300974 - Altora Pharma Solutions LLC - 2026-01-15](https://www.globalkeysolutions.net/records/fda_inspections/altora-pharma-solutions-llc/dfdc1c4f-b51b-4415-8cb4-a2486606441b) — classification: No Action Indicated (NAI), source: FDA, date: January 15, 2026
- [FDA Inspection 1205240 - Altora Pharma Solutions LLC - 2023-02-01](https://www.globalkeysolutions.net/records/fda_inspections/altora-pharma-solutions-llc/432c84fb-4764-4803-92f3-316bc0c136f4) — classification: No Action Indicated (NAI), source: FDA, date: February 1, 2023
- [FDA Inspection 1027725 - Altora Pharma Solutions LLC - 2017-08-18](https://www.globalkeysolutions.net/records/fda_inspections/altora-pharma-solutions-llc/564b7092-e932-42c7-a088-51d408b6f884) — classification: No Action Indicated (NAI), source: FDA, date: August 18, 2017
- [FDA Inspection 935302 - Altora Pharma Solutions LLC - 2015-03-31](https://www.globalkeysolutions.net/records/fda_inspections/altora-pharma-solutions-llc/f218afd6-e6f9-4f7a-bfc2-f0d53e1b90e7) — classification: No Action Indicated (NAI), source: FDA, date: March 31, 2015
- [FDA Inspection 935302 - Altora Pharma Solutions LLC - 2015-03-31](https://www.globalkeysolutions.net/records/fda_inspections/altora-pharma-solutions-llc/d6008a44-9b6a-49a0-963a-8a24c6eeaa1d) — classification: No Action Indicated (NAI), source: FDA, date: March 31, 2015

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