# Diteba Inc – FDA Inspection, Jul 5, 2019

Source: https://www.keypedia.com/records/fda_inspections/diteba-inc/417ad912-ceea-4666-8394-0258925e134f
Source feed: FDA_Inspections

> FDA inspection 1095508 of Diteba Inc, July 05, 2019. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 211. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1095508
- Company Name: Diteba Inc
- Inspection Date: 2019-07-05
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: New Drug Evaluation
- Product Type: Human Drugs
- Center: Human Drugs
- Office Name: Office of Inspections and Investigations
- Citation Count: 1

## Related Documents

- FDA Inspection 1112231 - 2019-11-15
- FDA Inspection 1025577 - 2017-08-04
- [FDA Inspection 904706 - 2014-10-29](https://www.keypedia.com/records/fda_inspections/diteba-inc/6e441bdf-6eba-45a6-8a1a-20007c2f8493)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/erik-w-koester/2bbab081-6783-40a1-83c1-b219bde22bd1)

Company: https://www.keypedia.com/companies/diteba-inc/b417709d-a31b-4336-b459-c95e78e72b78

Office: https://www.keypedia.com/offices/office-of-inspections-and-investigations/7dd0b904-a3df-46bc-a7b2-70ddb6f809c8