# PROMEPLA – FDA Inspection, May 16, 2018

Source: https://www.keypedia.com/records/fda_inspections/promepla/d8fc4fac-8825-488d-94e0-eb86adcf0f84
Source feed: FDA_Inspections

> FDA inspection 1053190 of PROMEPLA, May 16, 2018. 1 citation under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1053190
- Company Name: PROMEPLA
- Inspection Date: 2018-05-16
- Project Area: Compliance: Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations
- Citation Count: 1

## Related Documents

- [FDA Inspection 1244236 - 2024-07-18](https://www.keypedia.com/records/fda_inspections/promepla/e1385f60-1b4f-4f9b-a50d-9871cf242696)
- [FDA Inspection 864181 - 2013-12-12](https://www.keypedia.com/records/fda_inspections/promepla/6f888c99-ae61-4eb0-a5b1-9d19c158b4d0)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/ronald-ifraimov/b4ce8b79-3fa2-4862-b7a4-68e14e45d87a)

Company: https://www.keypedia.com/companies/promepla/e75790ce-8af4-4a01-8612-f6d7f462cfc3

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