# Decatur Memorial Hospital - PET Production - Inspection Records

Source: https://www.globalkeysolutions.net/companies/decatur-memorial-hospital-pet-production/755cb4e5-752d-48d3-8f05-d44ef576276a

> Inspection records and compliance data for Decatur Memorial Hospital - PET Production in Decatur, Illinois. Access full analysis and detailed observations.

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## Details

- Name: Decatur Memorial Hospital - PET Production
- FEI Number: 3009754344
- City: Decatur
- State: Illinois
- Country Name: United States
- Address Line 1: 2300 N Edward St Ste 100
- Zip Code: 62526
- Business Operations: POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION

## Related Documents

- [483 - Decatur Memorial Hospital - PET Production - 2026-01-15](https://www.globalkeysolutions.net/records/483/decatur-memorial-hospital-pet-production/873a8304-1826-4757-9bb8-cadcd6f330ca) — source: FDA, date: January 15, 2026
- [FDA Inspection 1299318 - Decatur Memorial Hospital - PET Production - 2026-01-15](https://www.globalkeysolutions.net/records/fda_inspections/decatur-memorial-hospital-pet-production/61406f2c-1512-463a-85d4-d65e2fac79cf) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 15, 2026
- [FDA Inspection 984042 - Decatur Memorial Hospital - PET Production - 2016-08-17](https://www.globalkeysolutions.net/records/fda_inspections/decatur-memorial-hospital-pet-production/69d1aaed-c1ee-4ef2-ac50-e56038ffb959) — classification: No Action Indicated (NAI), source: FDA, date: August 17, 2016
- [FDA Inspection 905438 - Decatur Memorial Hospital - PET Production - 2014-12-05](https://www.globalkeysolutions.net/records/fda_inspections/decatur-memorial-hospital-pet-production/7aa86fe9-19ee-442b-926e-e6159a093c24) — classification: No Action Indicated (NAI), source: FDA, date: December 5, 2014
- [FDA Inspection 805868 - Decatur Memorial Hospital - PET Production - 2012-10-24](https://www.globalkeysolutions.net/records/fda_inspections/decatur-memorial-hospital-pet-production/460285af-1a0c-4fc2-ad28-c489700d7807) — classification: No Action Indicated (NAI), source: FDA, date: October 24, 2012

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