# FDA Inspection 1069053 - Ocusoft Inc. - October 17, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/ocusoft-inc/613507d2-efa0-41e6-8ff1-7e8a2a7790b6
Source feed: FDA_Inspections

> FDA Inspection 1069053 for Ocusoft Inc. on October 17, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1069053
- Company Name: Ocusoft Inc.
- Inspection Date: 2018-10-17
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Office Name: Center for Drug Evaluation and Research

## Related Documents

- [FDA Inspection 995258 - 2016-12-14](https://www.globalkeysolutions.net/records/fda_inspections/ocusoft-inc/35f2bf74-69e5-4a27-b401-0a564fa7a6da)
- [FDA Inspection 824806 - 2013-03-28](https://www.globalkeysolutions.net/records/fda_inspections/ocusoft-inc/5282107c-5958-4507-819f-af694967ab46)
- [FDA Inspection 824806 - 2013-03-28](https://www.globalkeysolutions.net/records/fda_inspections/ocusoft-inc/04e35f0c-251c-4fdb-a7b4-7313a3775be2)

Company: https://www.globalkeysolutions.net/companies/ocusoft-inc/5ea7f1ef-b7ea-4fd4-bc64-7ebb93256098

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