FDA Inspection
NARANG MEDICAL USA CORPORATIONNARANG MEDICAL USA CORPORATION – FDA Inspection, Mar 22, 2018
Record Details
This FDA Inspection record concerns NARANG MEDICAL USA CORPORATION, with an inspection on March 22, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · af24de98-4d27-4274-b945-3f408af47b41
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1045233
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
- Outcome
- Form 483 issued
FDA Citations
4- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.50Purchasing controls, Lack of or inadequate procedures
- 21 CFR 820.30(j)Design history file
- 21 CFR 803.17Lack of Written MDR Procedures
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Other FDA inspections of NARANG MEDICAL USA CORPORATION
2| Date | Classification | Office | Project area |
|---|---|---|---|
| July 1, 2026 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 17, 2023 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for NARANG MEDICAL USA CORPORATION
- FDA Inspection 1325692 - 2026-07-01
- FDA Inspection 1206562 - 2023-03-17
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