# ARUP Laboratories, Inc. – FDA Inspection, Jul 14, 2017

Source: https://www.keypedia.com/records/fda_inspections/arup-laboratories-inc/ffb9e5eb-304c-495c-b633-05064b2e0e9c
Source feed: FDA_Inspections

> FDA inspection 1036656 of ARUP Laboratories, Inc., July 14, 2017. Form 483 issued. 8 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1036656
- Company Name: ARUP Laboratories, Inc.
- Inspection Date: 2017-07-14
- Product Type: Human Drugs
- Center: Human Drugs
- Office Name: Denver District Office
- Citation Count: 0

## Related Documents

- [FDA Inspection 1295758 - 2025-12-17](https://www.keypedia.com/records/fda_inspections/arup-laboratories-inc/3ec24c68-5c6d-4fcd-9b4a-a3555b7228ca)
- FDA Inspection 1294066 - 2025-12-04
- FDA Inspection 1086864 - 2019-03-11
- [FDA Inspection 998801 - 2016-11-18](https://www.keypedia.com/records/fda_inspections/arup-laboratories-inc/ac6343e0-10d4-4eca-ae68-ddfae4dca9e7)
- FDA Inspection 911879 - 2015-01-30

## Related Officers

- Issuing Officer

Company: https://www.keypedia.com/companies/arup-laboratories-inc/5aba7097-90ba-4744-a156-5354d35b65f7

Office: https://www.keypedia.com/offices/denver-district-office/93b79063-390c-4759-af6c-5da7e388face