FDA Inspection
THE KAMA SUTRA COMPANYTHE KAMA SUTRA COMPANY – FDA Inspection, Dec 11, 2018
Record Details
This FDA Inspection record concerns THE KAMA SUTRA COMPANY, with an inspection on December 11, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · fe449e2f-fc51-46a0-bc3b-0c4febab2950
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1074135
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 820.20(c)Management review dates
Full citation text and observation details available on the Dashboard.
Other FDA inspections of THE KAMA SUTRA COMPANY
1| Date | Classification | Office | Project area |
|---|---|---|---|
| March 31, 2022 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for THE KAMA SUTRA COMPANY
- FDA Inspection 1167662 - 2022-03-31
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