# FDA Inspection 1097339 - Remington Davis Inc - July 10, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/remington-davis-inc/dd217eed-8c5a-457c-8511-29dc271c80dc
Source feed: FDA_Inspections

> FDA Inspection 1097339 for Remington Davis Inc on July 10, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1097339
- Company Name: Remington Davis Inc
- Inspection Date: 2019-07-10
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Drugs
- Office Name: Center for Drug Evaluation and Research

## Related Documents

- [FDA Inspection 1072627 - 2018-10-22](https://www.globalkeysolutions.net/records/fda_inspections/remington-davis-inc/882b6884-735a-48c5-b9b4-f87a861f22ce)
- [FDA Inspection 1002423 - 2017-01-27](https://www.globalkeysolutions.net/records/fda_inspections/remington-davis-inc/9008a8ef-3be7-4d89-9302-5009fbd908c5)

Company: https://www.globalkeysolutions.net/companies/remington-davis-inc/4aea681a-cbf8-4dfa-abb3-2a6a6091c06f

Office: https://www.globalkeysolutions.net/offices/center-for-drug-evaluation-and-research/cd980d74-1cbf-4226-ba9a-9045324c236c