# N-Molecular, Inc. dba SOFIE - Inspection Records

Source: https://www.globalkeysolutions.net/companies/n-molecular-inc-dba-sofie/174feca7-eb92-4be2-a81d-4f7c2697b112

> Inspection records and compliance data for N-Molecular, Inc. dba SOFIE in Colonie, New York. Access full analysis and detailed observations.

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## Details

- Name: N-Molecular, Inc. dba SOFIE
- FEI Number: 3008302705
- City: Colonie
- State: New York
- Country Name: United States
- Address Line 1: 25 Walker Way Ste D
- Zip Code: 12205
- Business Operations: POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION

## Related Documents

- [FDA Inspection 1290166 - N-Molecular, Inc. dba SOFIE - 2026-02-05](https://www.globalkeysolutions.net/records/fda_inspections/n-molecular-inc-dba-sofie/f323549d-300c-4a2f-8f44-5515bb1047e8) — source: FDA, date: February 5, 2026
- [FDA Inspection 1290166 - N-Molecular, Inc. dba SOFIE - 2026-02-05](https://www.globalkeysolutions.net/records/fda_inspections/n-molecular-inc-dba-sofie/7a93361e-d11b-456e-8441-2c80be8b2549) — classification: No Action Indicated (NAI), source: FDA, date: February 5, 2026
- [483 - N-Molecular, Inc. dba SOFIE - 2020-01-13](https://www.globalkeysolutions.net/records/483/n-molecular-inc-dba-sofie/81a5c5d1-39a2-4215-8d0a-e9f50174e667) — source: FDA, date: January 13, 2020
- [FDA Inspection 1115024 - N-Molecular, Inc. dba SOFIE - 2020-01-13](https://www.globalkeysolutions.net/records/fda_inspections/n-molecular-inc-dba-sofie/0e5bd43a-8283-4d63-bbf8-6a0e2f429d73) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 13, 2020
- [FDA Inspection 913744 - N-Molecular, Inc. dba SOFIE - 2015-02-12](https://www.globalkeysolutions.net/records/fda_inspections/n-molecular-inc-dba-sofie/f779ffc5-77fe-4af2-a053-8edb433e1ad1) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 12, 2015
- [FDA Inspection 754503 - N-Molecular, Inc. dba SOFIE - 2011-11-14](https://www.globalkeysolutions.net/records/fda_inspections/n-molecular-inc-dba-sofie/049b7c5a-5b61-4f7b-83bf-e7da39db8a13) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 14, 2011

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