# Tokuhon Corporation Miyashiro Factory – FDA Inspection, Nov 4, 2016

Source: https://www.keypedia.com/records/fda_inspections/tokuhon-corporation-miyashiro-factory/d5a09f86-2792-41d5-838b-e0cfa8c0a97c
Source feed: FDA_Inspections

> FDA inspection 995997 of Tokuhon Corporation Miyashiro Factory, November 04, 2016. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 211. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 995997
- Company Name: Tokuhon Corporation Miyashiro Factory
- Inspection Date: 2016-11-04
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Center: Human Drugs
- Office Name: Center for Drug Evaluation and Research
- Citation Count: 3

## Related Documents

- [FDA Inspection 749511 - 2011-09-23](https://www.keypedia.com/records/fda_inspections/tokuhon-corporation-miyashiro-factory/be4ef16e-3054-4f99-8cb0-89fe7168307e)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/erika-v-butler/3e654530-4c29-403d-880e-a5422315c3c0)

Company: https://www.keypedia.com/companies/tokuhon-corporation-miyashiro-factory/59dd37b2-71ac-4be9-bfb9-6ca3b0260f13

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