# FDA Inspection 848000 - FujiFilm Diosynth Biotechnologies U.S.A., Inc. - September 12, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/fujifilm-diosynth-biotechnologies-usa-inc/70820fec-b5a9-468f-97f1-c5caf7ee385e/
Source feed: FDA_Inspections

> FDA Inspection 848000 for FujiFilm Diosynth Biotechnologies U.S.A., Inc. on September 12, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 848000
- Company Name: FujiFilm Diosynth Biotechnologies U.S.A., Inc.
- Inspection Date: 2013-09-12
- Classification: No Action Indicated (NAI)
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Office Name: Center for Drug Evaluation and Research

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Company: https://www.globalkeysolutions.net/companies/fujifilm-diosynth-biotechnologies-usa-inc/44b7fa9f-848c-4e30-869e-12ddcfd848f8

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