FDA Inspection
E K Industries IncE K Industries Inc – FDA Inspection, Jun 2, 2016
Record Details
This FDA Inspection record concerns E K Industries Inc, with an inspection on June 2, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- E K Industries Inc
- Inspection Date
- June 2, 2016
- Product Type
- Devices
View Company Profile
ID · f116bd4f-c1e5-4646-8a64-eb13e110f815
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 976158
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.22Quality Audit/Reaudit - conducted
- 21 CFR 820.20(c)Management review dates
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