Anhui Jbh Medical Apparatus Co., Ltd. FDA Record

Warning letters, Form 483s, inspections, recalls and 510(k) clearances

  • Latest inspection VAI · Sep 11, 2025
  • No warning letters matched by name
Inspections 1 0 OAI
Recalls 0 0 Class I
Warning letters 0 None on file
510(k) clearances 14 Latest Oct 14, 2026

Anhui Jbh Medical Apparatus Co., Ltd. has 0 FDA recalls, 1 inspection, 14 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Anhui Jbh Medical Apparatus Co., Ltd." is on file.

What these totals cover: FDA records filed under the name "Anhui Jbh Medical Apparatus Co., Ltd." and its spelling variant "Anhui Jbh Medical Apparatus Co".

Latest inspection
Sep 11, 2025 · VAI
Latest 510(k)
Oct 14, 2026

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances14Nov 8, 2026File dated Nov 2, 2026Current
Inspections1Nov 14, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

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Recent FDA inspections

1 inspection on Sep 11, 2025.

DateSiteProductClassificationFEI
Sep 11, 2025Chuzhou, ChinaDevicesVoluntary Action Indicated (VAI)3016969129
NAI
No objectionable conditions or practices were found during the inspection.
VAI
Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
OAI
Regulatory and/or administrative actions are recommended.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

FDA-inspected facilities

1 inspected site, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3016969129Chuzhou, China1Sep 11, 2025

Recent 510(k) clearances

14 510(k) clearances from May 14, 2021 to Oct 14, 2026.

K-NumberDeviceDate
K261169Power Wheelchair (D39)Oct 14, 2026
K261200Power Wheelchair (D60)Oct 6, 2026
K261079Power Wheelchair (DC12)Oct 6, 2026
K261078Electric Scooter (FNS01,FNS03)Sep 24, 2026
K261859Electric Scooter (FDB08, FDB08A, FDB12)Sep 19, 2026
K251606Power Wheelchair (D26)Jun 25, 2025
K241374Manual Wheelchair (S002, S004, S005, S006, S007, S008, S009)Feb 28, 2025
K242448Power Wheelchair (D03, D05, D06, D09, D11, D16, D22, D23, D26, D36)Jan 2, 2025
K242468Power Wheelchair (D10, D12, D15, D17, D20, D37)Dec 31, 2024
K242252Power WheelchairDec 27, 2024
K241854Power WheelchairOct 4, 2024
K212092Portable Folding Electric Wheelchair (Model: DC01)May 6, 2022
K212090Electric ScooterApr 22, 2022
K210302Disposable Medical maskMay 14, 2021

Anhui Jbh Medical Apparatus Co., Ltd. and the FDA: common questions

Has Anhui Jbh Medical Apparatus Co., Ltd. received an FDA warning letter?

No FDA warning letter addressed to the name "Anhui Jbh Medical Apparatus Co., Ltd." is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.

Has Anhui Jbh Medical Apparatus Co., Ltd. received an FDA Form 483?

FDA has not published a Form 483 for "Anhui Jbh Medical Apparatus Co., Ltd." in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Anhui Jbh Medical Apparatus Co., Ltd.?

The most recent FDA inspection on file ended Sep 11, 2025 at Chuzhou, China and was classified VAI. FDA has 1 inspection of Anhui Jbh Medical Apparatus Co., Ltd. on file.

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Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.