# FDA Inspection 995258 - Ocusoft Inc. - December 14, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/ocusoft-inc/35f2bf74-69e5-4a27-b401-0a564fa7a6da
Source feed: FDA_Inspections

> FDA Inspection 995258 for Ocusoft Inc. on December 14, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 995258
- Company Name: Ocusoft Inc.
- Inspection Date: 2016-12-14
- Classification: No Action Indicated (NAI)
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Office Name: Center for Drug Evaluation and Research

## Related Documents

- [FDA Inspection 1069053 - 2018-10-17](https://www.globalkeysolutions.net/records/fda_inspections/ocusoft-inc/613507d2-efa0-41e6-8ff1-7e8a2a7790b6)
- [FDA Inspection 824806 - 2013-03-28](https://www.globalkeysolutions.net/records/fda_inspections/ocusoft-inc/5282107c-5958-4507-819f-af694967ab46)
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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
