# Gelflex Laboratories – FDA Inspection, Nov 30, 2017

Source: https://www.keypedia.com/records/fda_inspections/gelflex-laboratories/914f4d82-d192-4950-9dc7-27673166940e
Source feed: FDA_Inspections

> FDA inspection 1032353 of Gelflex Laboratories, November 30, 2017. 2 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1032353
- Company Name: Gelflex Laboratories
- Inspection Date: 2017-11-30
- Project Area: Postmarket Assurance: Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations
- Citation Count: 2

## Related Documents

- FDA Inspection 916761 - 2015-01-30

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/andrea-a-branche/9ffe9b53-7963-49a6-be4e-25e644f1759f)

Company: https://www.keypedia.com/companies/gelflex-laboratories/c780b470-5359-47ca-92aa-7530ea259f8c

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