# Diacor, Inc, Mount Pleasant, UT – FDA Inspections

Source: https://www.keypedia.com/companies/diacor-inc/11688ab9-29f4-4edd-9d07-82c11bec238a

> Inspection records and compliance data for Diacor, Inc in Mount Pleasant, Utah. 4 FDA inspections on record, 1 Form 483, last inspected September 08, 2017.

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## Details

- Name: Diacor, Inc
- FEI Number: 1721113
- Address Line 1: 1236 S Airstrip Ln
- City: Mount Pleasant
- State: Utah
- Zip Code: 84647-2208
- Country Name: United States
- Address: 1236 S Airstrip Ln, Mount Pleasant, Utah 84647-2208, United States
- Country: United States

## Related Documents

- [483 - Diacor, Inc - 2019-10-03](https://www.keypedia.com/records/483/diacor-inc/58a0b546-a219-4588-9373-cae5bedd181c) — source: FDA, date: October 3, 2019
- FDA Inspection 1024795 - Diacor, Inc - 2017-09-08 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 8, 2017
- [FDA Inspection 1024795 - Diacor, Inc - 2017-09-08](https://www.keypedia.com/records/fda_inspections/diacor-inc/b00ee590-6683-465b-aa92-c608f937809f) — classification: No Action Indicated (NAI), source: FDA, date: September 8, 2017
- FDA Inspection 1024795 - Diacor, Inc - 2017-09-08 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 8, 2017
- [FDA Inspection 836648 - Diacor, Inc - 2013-06-19](https://www.keypedia.com/records/fda_inspections/diacor-inc/ec5df3dc-96c9-4df3-a1e2-f6325281814b) — classification: No Action Indicated (NAI), source: FDA, date: June 19, 2013
- FDA Inspection 836648 - Diacor, Inc - 2013-06-19 — classification: No Action Indicated (NAI), source: FDA, date: June 19, 2013
- FDA Inspection 671010 - Diacor, Inc - 2010-06-17 — classification: No Action Indicated (NAI), source: FDA, date: June 17, 2010
- FDA Inspection 592352 - Diacor, Inc - 2009-06-25 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 25, 2009
- [FDA Inspection 592352 - Diacor, Inc - 2009-06-25](https://www.keypedia.com/records/fda_inspections/diacor-inc/669fbcfc-086b-4f2a-8481-9e8076b26e7f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 25, 2009

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